S.668 - Federal Government

A bill to require the Food and Drug Administration to conduct consumer testing to determine the appropriateness of the current labeling requirements for indoor tanning devices and determine whether such requirements provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the skin, including skin cancer, and for other purposes.  

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  • Sponsor introductory remarks on measure. (CR S2178)
    02/16/2007
  • Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2178-2179)
    02/16/2007
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Federal Government
Last Update
10/11/2009
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