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FDA Inspection
•Zhejiang Charioteer Pharmaceutical Co. Ltd.•July 4, 2014

Zhejiang Charioteer Pharmaceutical Co. Ltd. – FDA Inspection, Jul 4, 2014

Record Details

This FDA Inspection record concerns Zhejiang Charioteer Pharmaceutical Co. Ltd., with an inspection on July 4, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Charioteer Pharmaceutical Co. Ltd.
Inspection Date
July 4, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 7073a138-8fb5-4a5a-b61e-52e9efb0df9a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
890582
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Charioteer Pharmaceutical Co. Ltd.

4
DateClassificationOfficeProject area
June 12, 2026Not classifiedOffice of Inspections and Investigations
November 8, 2024Not classifiedOffice of Inspections and Investigations
January 18, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 15, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Charioteer Pharmaceutical Co. Ltd.
  • FDA Inspection 1328192 - 2026-06-12
  • FDA Inspection 1257164 - 2024-11-08
  • FDA Inspection 1039806 - 2018-01-18
  • FDA Inspection 748165 - 2011-09-15

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