[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2003]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR211.89]

[Page 123]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 211--CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS--Table of Contents
 
    Subpart E--Control of Components and Drug Product Containers and 
                                Closures
 
Sec. 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.