Administrative Detention of Drugs Intended for Human or Animal Use
other · Food and Drug Administration · Rule · Published 2014-05-29 · Effective 2014-06-30 · 79 FR 30716
Document
Document number
2014-12458
Federal Register citation
79 FR 30716
CFR reference
21 CFR 1
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2014-05-29
Effective date
2014-06-30
HHS docket
Docket No. FDA-2013-N-0365
Abstract
The Food and Drug Administration (FDA or the Agency) is implementing administrative detention authority with respect to drugs intended for human or animal use as authorized by amendments made to the Federal Food, Drug, and Cosmetic Act (the FD&C Act) by the Food and Drug Administration Safety and Innovation Act (FDASIA). FDA's administrative detention authority with respect to drugs allows FDA to better protect the integrity of the drug supply chain. Specifically, FDA is able to administratively detain drugs encountered during an inspection that an authorized FDA representative conducting an inspection has reason to believe are adulterated or misbranded. This authority is intended to protect the public by preventing distribution or subsequent use of drugs encountered during inspections that are believed to be adulterated or misbranded, until FDA has had time to consider what action it should take concerning the drugs, and to initiate legal action, if appropriate.