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483
•Samsung Biologics Co., Ltd.

Samsung Biologics Co., Ltd. – FDA 483

Record Details

An FDA inspection of Samsung Biologics Co., Ltd. in Incheon, Korea, revealed significant deficiencies across multiple areas of their drug manufacturing operations. Key issues included inadequate data integrity controls in the MSAT laboratory, failures to follow written procedures for aseptic processing, and a deficient Quality Unit. The inspection also cited problems with equipment revalidation and facility maintenance, indicating a broad scope of non-compliance.

Company
Samsung Biologics Co., Ltd.
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Hyunjong Lee
  • Jiyun S. Oh
  • Dongdo D. Mckenzie
View Company Profile

ID · f77a8fa0-5e1a-49af-b52c-92b0e5e25865

Other documents for Samsung Biologics Co., Ltd.
  • 483 - 2025-05-27May 27, 2025
  • 483 - 2024-07-30July 30, 2024
  • EIR - 2024-07-30July 30, 2024
  • 483 - 2023-09-01September 1, 2023
  • 483 - 2023-02-20February 20, 2023

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