21 CFR 211.134 - Drug product inspection.

§ 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.

Title 21 published on 2014-04-01

no entries appear in the Federal Register after this date.

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