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. All medicated feed manufacturing facilities that are registered with the Food & Drug Administration as a"drug establishment" (see article on "FDA medicated feed mill license approval and medicated feed manufacturing requirements for medicated animal feeds") are subj ect to FDA inspection for compliance with the Current Good Manufacturing Practice regulations (cGMPs) for medicated feeds (21 CFR 225.10 through 225.115 [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.