21 CFR 820.60
Identification. This section left the CFR when the QMSR took effect on Feb 2, 2026; the text below is as of Feb 1, 2026.
- Inspections citing it: 120
- Of those classified, ended OAI: 26%
- Last cited: FY2025
Inspections Citing It by Fiscal Year
Sites in and outside the US, FY2017 to Oct 20, 2026.
Regulation Text
eCFR, as of Feb 1, 2026Each manufacturer shall establish and maintain procedures for identifying product during all stages of receipt, production, distribution, and installation to prevent mixups.
Recently Cited Sites
Newest inspections citing this section; each opens the site- Precision Optics Corporation, Inc.United States · Sep 11, 2025
- Hong Qiangxing (Shen Zhen) Electronics LimitedChina · Aug 7, 2025
- Carroll-Baccari IncUnited States · Aug 5, 2025
- NIMBLEHEART, INCUnited States · Jun 27, 2025
Counts are inspections with posted citations that cite any paragraph of the section, once per inspection, from FDA's Data Dashboard. OAI share is over inspections FDA finally classified. Text from eCFR, the official online CFR. FDA Data Dashboard and eCFR