Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter C - Drugs: General |
Part 211 - Current Good Manufacturing Practice for Finished Pharmaceuticals |
Subpart E - Control of Components and Drug Product Containers and Closures |
§ 211.89 - Rejected components, drug product containers, and closures.
Latest version.
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§ 211.89 Rejected components, drug product containers, and closures.
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.