§211.134. Drug product inspection.
21 C.F.R. § 211.134
Packaged and labeled products shall be examined during finishing operations to provide assurance that containers and packages in the lot have the correct label.
A representative sample of units shall be collected at the completion of finishing operations and shall be visually examined for correct labeling.
Results of these examinations shall be recorded in the batch production or control records.
Notes, amendments, and revision history
Authority
Authority: 21 U.S.C. 321, 351, 352, 355, 360b, 360ddd, 360ddd-1, 371, 374; 42 U.S.C. 216, 262, 263a, 264.
Source
Source: 43 FR 45077, Sept. 29, 1978, unless otherwise noted.