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483
•Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. (FDF Site)•April 3, 2018

Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. (FDF Site) – FDA 483, Apr 3, 2018

Record Details

An FDA inspection of Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. in Nanjing, China, revealed significant deficiencies in their manufacturing processes for sterile drug products. Observations included inadequate procedures for preventing microbiological contamination, deficiencies in environmental monitoring within aseptic processing areas, and a lack of validated control procedures for manufacturing processes. Additionally, the firm failed to adequately qualify suppliers for containers and closures by not verifying test results.

Company
Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. (FDF Site)
Inspection date
April 3, 2018
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Rose Xu, Reviewer
  • Darren S. Brown (Consumer Safety Officer)
  • Djamila Harouaka (Microbiologist)
View Company Profile

ID · 5067c57b-7e67-4f78-87ab-a42f4d4b0b5c

Other documents for Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd. (FDF Site)
  • 483 - 2026-05-15May 15, 2026
  • 483 - 2025-12-15December 15, 2025

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