Deck 17: Consumer-Protection

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Question
A 2016 amendment to the Agricultural Marketing Act requires food producers to label food products that contain genetically modified organisms (GMOs).
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Question
Congress has made it a federal crime to engage in the extortionate extension of credit.
Question
The U.S.Food and Drug Administration inspects facilities engaged in egg production.
Question
Under the Controlling the Assault of Non-Solicited Pornography and Marketing Act of 2003 (the CAN-SPAM Act),online merchants cannot transfer a customer's payment information to a third-party merchant for a separate online sale without first obtaining the customer's consent to the transfer.
Question
Bitcoin gift cards are highly regulated currency and can be used with Amazon,Best Buy,and iTunes.
Question
In CASE 17.1 United States v.DeCoster (2016),the court held that a corporate officer is held liable for failure to take necessary measures to prevent or remedy violations of the Food,Drug,and Cosmetic Act,regardless of whether they were aware of or intended to cause the violation.
Question
The FDA has authority to regulate certain manufacturing aspects of tobacco,but it cannot regulate marketing of cigarettes or nicotine.
Question
In general,consumer protection law at the state level is more stringent than federal law.
Question
Executive branch regulatory agencies are located in cabinet departments.
Question
The Drug Quality and Security Act,enacted in 2013,made the compounding of drugs illegal.
Question
The Flammable Fabrics Act is an example of a federal law regulating the labeling of clothing.
Question
The Federal Commerce Commission has adopted guidelines specifying when manufacturers and marketers can label their products "Made in USA."
Question
The Fair Debt Collection Practices Act applies only to third-party debt collectors.
Question
The labeling of medical devices is under the jurisdiction of the Food and Drug Administration.
Question
If a used car is sold without a warranty,the label must state that the car is being sold "as is" as part of the FTC-required Buyer's Guide label.
Question
States may regulate odometer tampering,but there is no federal law that does so.
Question
The Fair Credit Reporting Act gives consumers a right to have corrected copies of their credit reports sent to creditors.
Question
Generic drugs can be approved for use on a showing that they are identical to approved brand-name drugs.
Question
The Truth-in-Lending Act (TILA)is intended to assure a truthful loan application by the consumer.
Question
Courts usually consider advertisements to be only an offer to deal.
Question
Which of the following categories of drugs cannot be approved by the Food and Drug Administration?

A) Schedule I
B) Schedule C
C) Schedule 2
D) Schedule D
Question
Under the Magnuson-Moss Warranty Act,a seller who offers a written warranty on goods must provide a full warranty.
Question
The Food and Drug Administration shares responsibility with the __________ for regulating pesticide residues on food.

A) Department of Agriculture
B) Department of Insecticide
C) Federal Trade Commission
D) Environmental Protection Agency
Question
The Consumer Credit Protection Act limits the garnishment of wages to the lesser of _____ of the debtor's disposable earnings for the week or the amount by which disposable earnings for the week exceed _____ times the current federal minimum hourly wage.

A) 10%; 30
B) 25%; 30
C) 30%; 25
D) 35%; 40
Question
Which of the following is allowed to broadband providers,according to the Open Internet Rules that went into effect in 2015?

A) Blocking access to legal services or devices
B) Eliminating pay-for-play fast lanes
C) Providing paid prioritization over other Internet traffic for consideration
D) Throttling lawful Internet traffic based on content
Question
The Federal Trade Commission has _____ commissioners who serve for _____-year terms.

A) seven; four
B) ten; five
C) six; six
D) five; seven
Question
The Truth-in-Lending Act provides consumers a right of __________ whenever their home is used as collateral for credit except for original construction or acquisition.

A) rescission
B) redemption
C) new mortgage
D) refinance
Question
Which of the following is NOT true regarding bioengineered insects and pathogens?

A) Scientists have created genetically engineered insects and microbes to fight pests that harm crops.
B) The Environmental Protection agency issues permits for the use of bioengineered insects.
C) The Food and Drug Administration issues permits for the use of bioengineered pathogens.
D) The Environmental Protection Agency issues permits for the use of bioengineered pathogens.
Question
A car loan is an example of a closed-end credit transaction.
Question
Before implementing a mandatory safety standard,the Consumer Product Safety Commission must find that __________ are inadequate.

A) voluntary standards
B) safety guidelines
C) product designs
D) warnings
Question
Caveat emptor means:

A) "let the buyer beware."
B) "let the buyer prevail."
C) "let the market decide."
D) "let the seller beware."
Question
The FDA sets _____ standards for what is considered adulterated natural foods.

A) mislabeling
B) unavoidable
C) zero tolerance
D) minimum tolerance
Question
Caveat venditor means:

A) "let the buyer beware."
B) "let the buyer prevail."
C) "let the market decide."
D) "let the seller beware."
Question
Which of the following is true regarding the Equal Credit Opportunity Act?

A) It prohibits discrimination against credit applicants based on gender and marital status.
B) It does not apply to applicants who derive their income from public assistance.
C) It applies only to business credit.
D) It applies only to consumer credit.
Question
The __________ has the primary responsibility for regulating the packaging and labeling of commodities other than food,drugs,medical devices,and cosmetics.

A) Federal Commerce Commission
B) Federal Interstate Regulating Commission
C) Federal Trade Commission
D) Uniform Commodity Commission
Question
The Truth-in-Lending Act limits credit card liability to $50 per card for unauthorized charges made before a card issuer is notified of a lost or stolen card.
Question
Point-of-purchase nutrition information labeling is voluntary for:

A) many raw foods.
B) vending machine products.
C) packages containing more than one serving.
D) food supplements that qualify as medicinal.
Question
Rules regarding the sale of e-cigarettes include all of the following EXCEPT:

A) purchaser must be 18 or older.
B) anyone under the age of 27 must show photo identification before being allowed to purchase tobacco products.
C) free samples are allowed to those over 18 showing photo identification.
D) vending machine sales are generally prohibited.
Question
Which of the following is NOT true regarding the use of genetically modified foods internationally?

A) The European Parliament refused to approve legislation requiring the labeling of genetically modified foods.
B) Australia requires the labeling of genetically modified food.
C) The only GMO crop China grows is cotton.
D) In New Zealand,if a genetically modified ingredient is "highly refined," the labeling requirements concerning GMOs do not apply.
Question
Under the FTC's __________,"all or virtually all" of the product must be made in the fifty states,the District of Columbia,or the U.S.territories and possessions.​

A) ​Made in USA policy
B) ​Made within USA policy
C) ​Wood Products Labeling Act
D) ​Labeling Preemption Act
Question
Which of the following are protected categories under the Equal Credit Opportunity Act?

A) Gender,race,color,religion,and national origin
B) Gender,race,color,religion,national origin,and age
C) Gender,marital status,race,color,religion,national origin,and age
D) Gender,marital status,race,color,religion,national origin,age,and residents of disadvantaged neighborhoods
Question
Discuss the purpose of the purpose of the Consumer Product Safety Commission and the process by which it sets mandatory safety standards.Discuss fully.
Question
Which of the following is true regarding FDA approval of medical devices in relation to state law claims for failure to warn?

A) FDA approval of medical devices does not preempt state failure-to-warn claims arising out of injuries caused by the device.
B) FDA approval of medical devices preempts state failure-to-warn claims arising out of injuries caused by the device,regardless of whether the device was exempted from full review.
C) FDA approval of medical devices preempts state failure-to-warn claims arising out of injuries caused by the device,unless the device was exempted from full review.
D) FDA approval of certain medical devices does not preempt state failure-to-warn claims arising out of injuries caused by the device,but federal law preempts state failure-to-warn claims related to nonapproved devices.
Question
The FTC now requires used car sellers to affix a __________ to the cars that they sell.

A) fixed price
B) buyer's guide
C) base price
D) discount price
Question
Which of the following is true regarding the use of irradiated foods in the United States?

A) Irradiated foods are outlawed.
B) Irradiation is allowed only for fruits and vegetables,and no notice is required.
C) Irradiation is allowed for fresh and frozen red meat,and no notice is required.
D) Irradiation is allowed for a variety of fresh and frozen meat,fruits,and vegetables,but must be labeled as treated.
Question
In general,when will the FDA require prescription use of a drug?

A) If the drug is toxic,requires a physician's supervision for safe use,or is addictive
B) Only if the drug is toxic
C) Only if the drug is either toxic or requires a physician's supervision for safe use
D) Only if the drug is addictive or requires a physician's supervision for safe use
Question
Which,according to the Food and Drug Administration,of the following is part of the definition of a drug?

A) Articles used for food or drink for humans or other animals
B) Chewing gum
C) Articles intended to affect the function of the body
D) Articles used for components of drink
Question
The Federal Trade Commission's "Guides for the Use of Environmental Marketing Claims" include all of the following EXCEPT:

A) the requirement of scientific testing necessary to substantiate environmental claims.
B) the application of the scientific validity of a consumer's belief as the standard for reasonableness.
C) the requirement of the marketer to specify whether the claim applies to the entire product,its packaging,a service,or a portion of those components.
D) a prohibition against the overstatement of any benefits claimed.
Question
Drug Company X has a prescription drug that will make people look younger and lose weight.The problem is that it causes significant stomach problems.Arden,an executive of Drug Company X,wants to advertise the drug's benefits on television and radio but leave out the stomach problems.Arden's secretary,Beck,warns that Arden could run into problems and is not sure the drug can even be advertised.Arden disagrees,stating that it is up to physicians to warn patients of possible complications.Arden decides not to provide any information regarding contacting Company X so that no one at Company X will be annoyed by receiving numerous inquiries about obtaining the drug's benefits.What would an FDA representative likely say in regard to Arden's plan? Provide your response in detail.
Question
Which of the following is true regarding the placement of health claims for foods on labels?

A) The FDA permits health food claims on labels without FDA approval as a new drug or the risk of sanctions for issuing a misbranded product,as long as the claim has been certified by the FDA as being supported by significant scientific agreement.
B) The FDA disallows health food claims on labels unless the food has been approved by the FDA as a type of new drug for the health concern involved.
C) The FDA allows health food claims on labels so long as the claim has not been certified by the FDA as false and misleading.
D) The FDA allows health food claims on labels without prior approval of the FDA only for organically grown foods.
Question
Which of the following is true regarding USDA standards for organic food?

A) Pesticides,genetic engineering,growth hormones,or irradiation may not be used.
B) Pesticides may be used,but genetic engineering and the use of growth hormones is disallowed.
C) Pesticides and irradiation may not be used,but genetic engineering and the use of growth hormones is allowed.
D) The USDA has no standards for organic food.
Question
_____ is the legal procedure by which a creditor may collect a debt by attaching a portion of a debtor's weekly wages.

A) Rescission
B) Garnishment
C) Joinder
D) Attachment
Question
Set forth the four main provisions of the CAN-SPAM Act.
Question
The first step in the FDA approval process for new drugs is their classification by the __________ based on currently accepted medical use and potential for abuse.

A) National Institute of Health
B) The Consumer Product Safety Commission
C) Drug Enforcement Administration
D) Congress
Question
What is the purpose of the Truth in Lending Act? What does it provide regarding the liability of credit cardholders for unauthorized charges when a card is lost or stolen?
Question
In 2014,the _______ announced it considered ______ to be a convertible virtual currency.

A) Wall Street Protection Group; ETF funds
B) Consumer Financial Protection Bureau; bitcoin
C) Internal Revenue Service; bitcoin
D) Internal Revenue Service; gold
Question
In CASE 17.2,XYZ Two Way Radio Service,Inc.v.Uber Technologies,Inc.(2016),the court analyzed whether Uber's claims regarding background checks and safety constituted false advertising in violation of the Lanham Act,among other claims.How did the court rule?

A) The court held that Uber's statements were subjective claims that "cannot be proven true or false" and are actionable under the Lanham Act.
B) The court held that Uber's statements that were challenged in the suit were nonactionable puffery under the Lanham Act.
C) The court held that Uber's statements regarding its background checks were false or misleading.
D) The court agreed with XYZ Two Way Radio Service,Inc.'s claims that certain Uber statements constituted false advertising in violation of the Lanham Act.
Question
Which of the following is NOT an FDA requirement for food manufacturing and processing facilities?

A) Take preemptive measures to prevent contamination.
B) Identify foods at high risk for foodborne illness outbreaks.
C) Develop an electronic tracking system that follows food from "farm to fork."
D) Block foods from facilities outside the United States.
Question
The ______ controls the disclosure of credit terms so that the consumer will be able to compare more readily the various credit terms available and avoid the uninformed use of credit.

A) Fair Credit Billing Act
B) Equal Credit Opportunity Act
C) Fair Credit Reporting Act
D) Truth in Lending Act
Question
The __________ has primary responsibility for regulating the labeling of food.

A) Federal Trade Commission
B) Food and Drug Administration
C) The Consumer Product Safety Commission
D) The Federal Trade Commission
Question
Explain the Federal Trade Commission's current stand on ownership of broadcasting stations and why some consider it controversial.
Question
When does an advertiser violate the Federal Trade Commission bait and switch advertising rules?
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Deck 17: Consumer-Protection
1
A 2016 amendment to the Agricultural Marketing Act requires food producers to label food products that contain genetically modified organisms (GMOs).
True
2
Congress has made it a federal crime to engage in the extortionate extension of credit.
True
3
The U.S.Food and Drug Administration inspects facilities engaged in egg production.
False
4
Under the Controlling the Assault of Non-Solicited Pornography and Marketing Act of 2003 (the CAN-SPAM Act),online merchants cannot transfer a customer's payment information to a third-party merchant for a separate online sale without first obtaining the customer's consent to the transfer.
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
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k this deck
5
Bitcoin gift cards are highly regulated currency and can be used with Amazon,Best Buy,and iTunes.
Unlock Deck
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k this deck
6
In CASE 17.1 United States v.DeCoster (2016),the court held that a corporate officer is held liable for failure to take necessary measures to prevent or remedy violations of the Food,Drug,and Cosmetic Act,regardless of whether they were aware of or intended to cause the violation.
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
7
The FDA has authority to regulate certain manufacturing aspects of tobacco,but it cannot regulate marketing of cigarettes or nicotine.
Unlock Deck
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k this deck
8
In general,consumer protection law at the state level is more stringent than federal law.
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k this deck
9
Executive branch regulatory agencies are located in cabinet departments.
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k this deck
10
The Drug Quality and Security Act,enacted in 2013,made the compounding of drugs illegal.
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k this deck
11
The Flammable Fabrics Act is an example of a federal law regulating the labeling of clothing.
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k this deck
12
The Federal Commerce Commission has adopted guidelines specifying when manufacturers and marketers can label their products "Made in USA."
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k this deck
13
The Fair Debt Collection Practices Act applies only to third-party debt collectors.
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14
The labeling of medical devices is under the jurisdiction of the Food and Drug Administration.
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k this deck
15
If a used car is sold without a warranty,the label must state that the car is being sold "as is" as part of the FTC-required Buyer's Guide label.
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k this deck
16
States may regulate odometer tampering,but there is no federal law that does so.
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k this deck
17
The Fair Credit Reporting Act gives consumers a right to have corrected copies of their credit reports sent to creditors.
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k this deck
18
Generic drugs can be approved for use on a showing that they are identical to approved brand-name drugs.
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k this deck
19
The Truth-in-Lending Act (TILA)is intended to assure a truthful loan application by the consumer.
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k this deck
20
Courts usually consider advertisements to be only an offer to deal.
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k this deck
21
Which of the following categories of drugs cannot be approved by the Food and Drug Administration?

A) Schedule I
B) Schedule C
C) Schedule 2
D) Schedule D
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22
Under the Magnuson-Moss Warranty Act,a seller who offers a written warranty on goods must provide a full warranty.
Unlock Deck
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Unlock Deck
k this deck
23
The Food and Drug Administration shares responsibility with the __________ for regulating pesticide residues on food.

A) Department of Agriculture
B) Department of Insecticide
C) Federal Trade Commission
D) Environmental Protection Agency
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k this deck
24
The Consumer Credit Protection Act limits the garnishment of wages to the lesser of _____ of the debtor's disposable earnings for the week or the amount by which disposable earnings for the week exceed _____ times the current federal minimum hourly wage.

A) 10%; 30
B) 25%; 30
C) 30%; 25
D) 35%; 40
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Unlock for access to all 62 flashcards in this deck.
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25
Which of the following is allowed to broadband providers,according to the Open Internet Rules that went into effect in 2015?

A) Blocking access to legal services or devices
B) Eliminating pay-for-play fast lanes
C) Providing paid prioritization over other Internet traffic for consideration
D) Throttling lawful Internet traffic based on content
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Unlock for access to all 62 flashcards in this deck.
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26
The Federal Trade Commission has _____ commissioners who serve for _____-year terms.

A) seven; four
B) ten; five
C) six; six
D) five; seven
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27
The Truth-in-Lending Act provides consumers a right of __________ whenever their home is used as collateral for credit except for original construction or acquisition.

A) rescission
B) redemption
C) new mortgage
D) refinance
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
28
Which of the following is NOT true regarding bioengineered insects and pathogens?

A) Scientists have created genetically engineered insects and microbes to fight pests that harm crops.
B) The Environmental Protection agency issues permits for the use of bioengineered insects.
C) The Food and Drug Administration issues permits for the use of bioengineered pathogens.
D) The Environmental Protection Agency issues permits for the use of bioengineered pathogens.
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k this deck
29
A car loan is an example of a closed-end credit transaction.
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k this deck
30
Before implementing a mandatory safety standard,the Consumer Product Safety Commission must find that __________ are inadequate.

A) voluntary standards
B) safety guidelines
C) product designs
D) warnings
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
31
Caveat emptor means:

A) "let the buyer beware."
B) "let the buyer prevail."
C) "let the market decide."
D) "let the seller beware."
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Unlock Deck
k this deck
32
The FDA sets _____ standards for what is considered adulterated natural foods.

A) mislabeling
B) unavoidable
C) zero tolerance
D) minimum tolerance
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
33
Caveat venditor means:

A) "let the buyer beware."
B) "let the buyer prevail."
C) "let the market decide."
D) "let the seller beware."
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
34
Which of the following is true regarding the Equal Credit Opportunity Act?

A) It prohibits discrimination against credit applicants based on gender and marital status.
B) It does not apply to applicants who derive their income from public assistance.
C) It applies only to business credit.
D) It applies only to consumer credit.
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
35
The __________ has the primary responsibility for regulating the packaging and labeling of commodities other than food,drugs,medical devices,and cosmetics.

A) Federal Commerce Commission
B) Federal Interstate Regulating Commission
C) Federal Trade Commission
D) Uniform Commodity Commission
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k this deck
36
The Truth-in-Lending Act limits credit card liability to $50 per card for unauthorized charges made before a card issuer is notified of a lost or stolen card.
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Unlock Deck
k this deck
37
Point-of-purchase nutrition information labeling is voluntary for:

A) many raw foods.
B) vending machine products.
C) packages containing more than one serving.
D) food supplements that qualify as medicinal.
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Unlock Deck
k this deck
38
Rules regarding the sale of e-cigarettes include all of the following EXCEPT:

A) purchaser must be 18 or older.
B) anyone under the age of 27 must show photo identification before being allowed to purchase tobacco products.
C) free samples are allowed to those over 18 showing photo identification.
D) vending machine sales are generally prohibited.
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
39
Which of the following is NOT true regarding the use of genetically modified foods internationally?

A) The European Parliament refused to approve legislation requiring the labeling of genetically modified foods.
B) Australia requires the labeling of genetically modified food.
C) The only GMO crop China grows is cotton.
D) In New Zealand,if a genetically modified ingredient is "highly refined," the labeling requirements concerning GMOs do not apply.
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
40
Under the FTC's __________,"all or virtually all" of the product must be made in the fifty states,the District of Columbia,or the U.S.territories and possessions.​

A) ​Made in USA policy
B) ​Made within USA policy
C) ​Wood Products Labeling Act
D) ​Labeling Preemption Act
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
41
Which of the following are protected categories under the Equal Credit Opportunity Act?

A) Gender,race,color,religion,and national origin
B) Gender,race,color,religion,national origin,and age
C) Gender,marital status,race,color,religion,national origin,and age
D) Gender,marital status,race,color,religion,national origin,age,and residents of disadvantaged neighborhoods
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42
Discuss the purpose of the purpose of the Consumer Product Safety Commission and the process by which it sets mandatory safety standards.Discuss fully.
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Unlock Deck
k this deck
43
Which of the following is true regarding FDA approval of medical devices in relation to state law claims for failure to warn?

A) FDA approval of medical devices does not preempt state failure-to-warn claims arising out of injuries caused by the device.
B) FDA approval of medical devices preempts state failure-to-warn claims arising out of injuries caused by the device,regardless of whether the device was exempted from full review.
C) FDA approval of medical devices preempts state failure-to-warn claims arising out of injuries caused by the device,unless the device was exempted from full review.
D) FDA approval of certain medical devices does not preempt state failure-to-warn claims arising out of injuries caused by the device,but federal law preempts state failure-to-warn claims related to nonapproved devices.
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
44
The FTC now requires used car sellers to affix a __________ to the cars that they sell.

A) fixed price
B) buyer's guide
C) base price
D) discount price
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
45
Which of the following is true regarding the use of irradiated foods in the United States?

A) Irradiated foods are outlawed.
B) Irradiation is allowed only for fruits and vegetables,and no notice is required.
C) Irradiation is allowed for fresh and frozen red meat,and no notice is required.
D) Irradiation is allowed for a variety of fresh and frozen meat,fruits,and vegetables,but must be labeled as treated.
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
46
In general,when will the FDA require prescription use of a drug?

A) If the drug is toxic,requires a physician's supervision for safe use,or is addictive
B) Only if the drug is toxic
C) Only if the drug is either toxic or requires a physician's supervision for safe use
D) Only if the drug is addictive or requires a physician's supervision for safe use
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
47
Which,according to the Food and Drug Administration,of the following is part of the definition of a drug?

A) Articles used for food or drink for humans or other animals
B) Chewing gum
C) Articles intended to affect the function of the body
D) Articles used for components of drink
Unlock Deck
Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
48
The Federal Trade Commission's "Guides for the Use of Environmental Marketing Claims" include all of the following EXCEPT:

A) the requirement of scientific testing necessary to substantiate environmental claims.
B) the application of the scientific validity of a consumer's belief as the standard for reasonableness.
C) the requirement of the marketer to specify whether the claim applies to the entire product,its packaging,a service,or a portion of those components.
D) a prohibition against the overstatement of any benefits claimed.
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Unlock for access to all 62 flashcards in this deck.
Unlock Deck
k this deck
49
Drug Company X has a prescription drug that will make people look younger and lose weight.The problem is that it causes significant stomach problems.Arden,an executive of Drug Company X,wants to advertise the drug's benefits on television and radio but leave out the stomach problems.Arden's secretary,Beck,warns that Arden could run into problems and is not sure the drug can even be advertised.Arden disagrees,stating that it is up to physicians to warn patients of possible complications.Arden decides not to provide any information regarding contacting Company X so that no one at Company X will be annoyed by receiving numerous inquiries about obtaining the drug's benefits.What would an FDA representative likely say in regard to Arden's plan? Provide your response in detail.
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50
Which of the following is true regarding the placement of health claims for foods on labels?

A) The FDA permits health food claims on labels without FDA approval as a new drug or the risk of sanctions for issuing a misbranded product,as long as the claim has been certified by the FDA as being supported by significant scientific agreement.
B) The FDA disallows health food claims on labels unless the food has been approved by the FDA as a type of new drug for the health concern involved.
C) The FDA allows health food claims on labels so long as the claim has not been certified by the FDA as false and misleading.
D) The FDA allows health food claims on labels without prior approval of the FDA only for organically grown foods.
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k this deck
51
Which of the following is true regarding USDA standards for organic food?

A) Pesticides,genetic engineering,growth hormones,or irradiation may not be used.
B) Pesticides may be used,but genetic engineering and the use of growth hormones is disallowed.
C) Pesticides and irradiation may not be used,but genetic engineering and the use of growth hormones is allowed.
D) The USDA has no standards for organic food.
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52
_____ is the legal procedure by which a creditor may collect a debt by attaching a portion of a debtor's weekly wages.

A) Rescission
B) Garnishment
C) Joinder
D) Attachment
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53
Set forth the four main provisions of the CAN-SPAM Act.
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54
The first step in the FDA approval process for new drugs is their classification by the __________ based on currently accepted medical use and potential for abuse.

A) National Institute of Health
B) The Consumer Product Safety Commission
C) Drug Enforcement Administration
D) Congress
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55
What is the purpose of the Truth in Lending Act? What does it provide regarding the liability of credit cardholders for unauthorized charges when a card is lost or stolen?
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56
In 2014,the _______ announced it considered ______ to be a convertible virtual currency.

A) Wall Street Protection Group; ETF funds
B) Consumer Financial Protection Bureau; bitcoin
C) Internal Revenue Service; bitcoin
D) Internal Revenue Service; gold
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57
In CASE 17.2,XYZ Two Way Radio Service,Inc.v.Uber Technologies,Inc.(2016),the court analyzed whether Uber's claims regarding background checks and safety constituted false advertising in violation of the Lanham Act,among other claims.How did the court rule?

A) The court held that Uber's statements were subjective claims that "cannot be proven true or false" and are actionable under the Lanham Act.
B) The court held that Uber's statements that were challenged in the suit were nonactionable puffery under the Lanham Act.
C) The court held that Uber's statements regarding its background checks were false or misleading.
D) The court agreed with XYZ Two Way Radio Service,Inc.'s claims that certain Uber statements constituted false advertising in violation of the Lanham Act.
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58
Which of the following is NOT an FDA requirement for food manufacturing and processing facilities?

A) Take preemptive measures to prevent contamination.
B) Identify foods at high risk for foodborne illness outbreaks.
C) Develop an electronic tracking system that follows food from "farm to fork."
D) Block foods from facilities outside the United States.
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59
The ______ controls the disclosure of credit terms so that the consumer will be able to compare more readily the various credit terms available and avoid the uninformed use of credit.

A) Fair Credit Billing Act
B) Equal Credit Opportunity Act
C) Fair Credit Reporting Act
D) Truth in Lending Act
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60
The __________ has primary responsibility for regulating the labeling of food.

A) Federal Trade Commission
B) Food and Drug Administration
C) The Consumer Product Safety Commission
D) The Federal Trade Commission
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61
Explain the Federal Trade Commission's current stand on ownership of broadcasting stations and why some consider it controversial.
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62
When does an advertiser violate the Federal Trade Commission bait and switch advertising rules?
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