S. 2192 · 110th Congress

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

Stage
In committee
Introduced
2007-10-18
Latest action
2007-10-18 · Introduced in Senate

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.