A bill to establish a user fee for follow-up reinspections under the Federal Food, Drug, and Cosmetic Act.

Summary

Directs the Secretary of Health and Human Services to collect a user fee from each manufacturer of a food, drug, device, biological product, or animal drug for which a followup reinspection is required to ensure correction of a violation of a Good Manufacturing Practices requirement under the Federal Food, Drug, and Cosmetic Act found by the Secretary during the initial inspection of the manufacturer.

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Timeline

1. 18 October 2007

   Introduced

   Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S13088)

   Source: IntroReferral

2. 18 October 2007

   Introduced

   Sponsor introductory remarks on measure. (CR S13087)

   Source: IntroReferral

3. 18 October 2007

   Introduced

   Introduced in Senate

   Source: IntroReferral

Votes

No vote records are attached yet.

Versions

• Introduced in Senate · 18 October 2007 · Official file

Documents

3 official files

• Introduced in Senate (text)

  Introduced in Senate · EN · 18 October 2007

  ViewDownloadOpen at official source

• Introduced in Senate (PDF)

  Introduced in Senate · EN · 18 October 2007

  ViewDownloadOpen at official source

• Introduced in Senate

  summary · EN · 18 October 2007

  Open at official source

Sponsors

• Sen. Feingold, Russell D. [D-WI] · D · Sponsor
• · sshr00 · Standing

Related records

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