21 CFR 820.60 : Food And Drugs (§ 1.1 To Parts 1403-1499) — (Subpart A To Parts 1272-1299) — Food And Drug Administration, Department Of Health And Human Services (Continued) (Subpart A To Parts 1272-1299) — Medical Devices (Subpart A To § 898.14) — Quality System Regulation (§ 820.1 To § 820.250) — Identification And Traceability (§ 820.60 And § 820.65) — Identification.
4 Aug 2016
Each manufacturer shall establish and maintain procedures for identifying product during all stages of receipt, production, distribution, and installation to prevent mixups.