Code of Federal Regulations · Section
§ 211.89 — Rejected Components, Drug Product Containers, And Closures
21 C.F.R. § 211.89
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Rejected components, drug product containers, and closures shall be identified and controlled under a quarantine system designed to prevent their use in manufacturing or processing operations for which they are unsuitable.
Authorizing Statute
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Definitions; generally21 U.S.C. § 321
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Regulations42 U.S.C. § 216