Preparing for, conducting and reacting to feed mill inspections

摘要

This article is intended to address Food & Drug Administration policy and current practices of industry relative to feed mill inspection activity. A 11 medicated feed manu-facturing facilities that are registered with the Food & Drug Administration asa "drug establishment" (see article on "FDA Approval Requirements for Use of Drugs in Animal Feeds") are subject to FDA inspection for compliance with the Current Good Manufacturing Practice regulations (cGMPs) for medicated feeds (21 CFR 225.10 through225.115 [sub-parts A through E]). Section 510 (1) (h) of the Federal Food, Drug, and Cosmetic (FD&C) Act mandates such inspections be conducted no less than once every two years.