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483
•Zhaoke Pharmaceutical (Hefei) Company Limited•June 18, 2024

Zhaoke Pharmaceutical (Hefei) Company Limited – FDA 483, Jun 18, 2024

Record Details

An FDA inspection of Zhaoke Pharmaceutical (Hefei) Company Limited, a sterile drug manufacturer in Hefei, China, revealed significant deficiencies across its operations. Observations included incomplete laboratory records for microbial counts, inadequate laboratory controls for endotoxin and filter integrity, and insufficient validation of aseptic and sterilization processes. The firm also failed to establish and follow proper aseptic procedures, maintain equipment, and ensure data integrity with audit trails.

Company
Zhaoke Pharmaceutical (Hefei) Company Limited
Inspection date
June 18, 2024
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Kejun Cheng (other)
  • Marcellinus D. Dordunoo (Investigator)
View Company Profile

ID · 9b01a5d7-d702-4c4e-8e30-d4f16a37a509

Other documents for Zhaoke Pharmaceutical (Hefei) Company Limited
  • EIR - 2024-06-18June 18, 2024

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