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483
•Alembic Pharmaceuticals Limited•March 24, 2023

Alembic Pharmaceuticals Limited – FDA 483, Mar 24, 2023

Record Details

Alembic Pharmaceuticals Limited, a sterile drug manufacturer, received a Form FDA 483 citing significant quality control deficiencies. Observations included the failure of the quality control unit to adequately review and approve drug product production records for contract manufactured batches prior to release. Additionally, the quality control unit lacked proper oversight, and internal audit procedures were found to be inadequate, with issues related to auditor training and audit scope.

Company
Alembic Pharmaceuticals Limited
Inspection date
March 24, 2023
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Nicole E. Knowlton (Investigator )
View Company Profile

ID · 7a4acca6-9c41-40e2-a37e-a19fe33c8bd5

Other documents for Alembic Pharmaceuticals Limited
  • 483 - 2026-02-18February 18, 2026
  • 483 - 2022-08-30August 30, 2022
  • 483 - 2021-10-28October 28, 2021
  • 483 - 2021-02-06February 6, 2021

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