[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: 21CFR211.134]

[Page 128]
 
                        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 G--Packaging and Labeling Control
 
Sec. 211.134  Drug product inspection.

    (a) Packaged and labeled products shall be examined during finishing 
operations to provide assurance that containers and packages in the lot 
have the correct label.
    (b) A representative sample of units shall be collected at the 
completion of finishing operations and shall be visually examined for 
correct labeling.
    (c) Results of these examinations shall be recorded in the batch 
production or control records.