Exam 19: Consumer Protection

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The Pure Food and Drug Act of 1906 was the first regulation of food and drugs. What sparked interest in this concern?

(Multiple Choice)
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Trade regulation rules tend to be issued in areas where the FTC thinks there are particular problems with deception.

(True/False)
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Medical devices approved by the FDA before being sold and then monitored for problems.

(True/False)
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When the Consumer Credit Protection Act was passed in 1968 there was about ____ worth of consumer credit outstanding.

(Multiple Choice)
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____ is a regulation written by the Federal Reserve Board specifying items that must be listed as part of consumer finance charges under the Truth-in-Lending Act.

(Multiple Choice)
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If you lose the bank card you use to withdraw cash from your bank by machine, and you report it to the bank within two days, you are liable for how much in losses?

(Multiple Choice)
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A possible benefit of drug regulations in place in many European nations is that:

(Multiple Choice)
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Which of the following is not a function of the Food and Drug Administration?

(Multiple Choice)
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The intent of the Nutrition Labeling and Education Act is to:

(Multiple Choice)
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In Chuway v. National Action Financial Services, where Chuway received a letter from debt collector National that requested payment of the amount she owed on a debt, the appeals court held that the debt collector:

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The government agency charged with monitoring food and drug safety is the:

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Truth in lending refers to the requirement that creditors:

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The FDA issues standards for nutrition labels on food.

(True/False)
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Which of these is most likely to be attacked by the FTC as a deceptive business practice?

(Multiple Choice)
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In Schuchmann v. Air Services Heating and Air Conditioning a home owner bought a heating and A/C unit with a lifetime warranty. After five years the company refused to honor the warranty because it was too expensive. When the consumer sued, the courts held that:

(Multiple Choice)
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In Wyeth v. Levine the Supreme Court held that FDA approval of the warning label on a drug did not mean the drug maker was not responsible for updating the label to include new relevant safety information.

(True/False)
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The Food, Drug and Cosmetic Act of 1938 did not expand the powers of the FDA to include:

(Multiple Choice)
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The FTC uses the ____ to put its policy about advertising into effect:

(Multiple Choice)
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The Food Quality Protection Act holds that a substance may be approved for use in food if:

(Multiple Choice)
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What is not a feature of the Consumer Credit Protection Act:

(Multiple Choice)
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