1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter C - DRUGS: GENERAL
  5. Part 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
  6. Subpart E - Control of Components and Drug Product Containers and Closures
  7. 21 CFR § 211.89
21 CFR § 211.89
Rejected components, drug product containers, and closures
June 25, 2020
CFR

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.

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§ 211.87 Retesting of approved components, drug product containers, and closures
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§ 211.94 Drug product containers and closures

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