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483
•Harbin Jixianglong Biotech Co., Ltd.•November 6, 2025

Harbin Jixianglong Biotech Co., Ltd. – FDA 483, Nov 6, 2025

Record Details

Harbin Jixianglong Biotech Co., Ltd. in Harbin, China, an API manufacturer, was cited for significant deficiencies during an FDA inspection. The observations highlight severe issues across quality control, manufacturing processes, data integrity, and documentation, indicating a lack of robust quality systems. These include distributing API without validation, inadequate laboratory controls, poor equipment cleaning, and insufficient computer system controls.

Company
Harbin Jixianglong Biotech Co., Ltd.
Inspection date
November 6, 2025
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Tekalign Wondimu ( Drug Investigator)
  • Bijoy Panicker
View Company Profile

ID · aa686475-905d-4681-8322-c5bf7aed7de0

Other documents for Harbin Jixianglong Biotech Co., Ltd.
  • WARNING_LETTER - 2025-11-07November 7, 2025

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