CFR 21-820.198-2013
Food and Drugs. Part820:Quality system regulation. Section820.198:Complaint files.

Standard No.

CFR 21-820.198-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-820.198-2013

Scope

(a) Each manufacturer shall maintain complaint files. Each manufacturer shall establish and maintain procedures for receiving, reviewing, and evaluating complaints by a formally designated unit. Such procedures shall ensure that:

CFR 21-820.198-2013 history

• 2013 CFR 21-820.198-2013 Food and Drugs. Part820:Quality system regulation. Section820.198:Complaint files.