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.
Introduced in Senate
Sponsor introductory remarks on measure. (CR S13087)
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S13088)
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