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FDA Inspection
•Huzhou Arthur Pharmaceutical Co., Ltd.•September 22, 2026

Huzhou Arthur Pharmaceutical Co., Ltd. – FDA Inspection, Sep 22, 2026

Record Details

This FDA Inspection record concerns Huzhou Arthur Pharmaceutical Co., Ltd., with an inspection on September 22, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Huzhou Arthur Pharmaceutical Co., Ltd.
Inspection Date
September 22, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Tekalign Wondimu (FDA Associated Person)
View Company Profile

ID · a2964c67-7ff0-4658-b32d-4665befa10ab

Inspection Facts

Inspection number
1337514
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Huzhou Arthur Pharmaceutical Co., Ltd.

2
DateClassificationOfficeProject area
June 19, 2026Not classifiedOffice of Inspections and Investigations
September 23, 2025OAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
Other documents for Huzhou Arthur Pharmaceutical Co., Ltd.
  • FDA Inspection 1328918 - 2026-06-19
  • FDA Inspection 1288564 - 2025-09-23

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