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FDA Inspection
•Huzhou Zhanwang Pharmaceutical Co., Ltd.•March 29, 2024

Huzhou Zhanwang Pharmaceutical Co., Ltd. – FDA Inspection, Mar 29, 2024

Record Details

This FDA Inspection record concerns Huzhou Zhanwang Pharmaceutical Co., Ltd., with an inspection on March 29, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Huzhou Zhanwang Pharmaceutical Co., Ltd.
Inspection Date
March 29, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Damaris Y. Hernandez (Investigator)
  • Suzanne N. Vallez (FDA Associated Person)
View Company Profile

ID · 5587637b-649c-4642-b8b3-ef1a785ddaf9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1237589
FDA center
Human Drugs
Project area
Drug Quality Assurance

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

3
DateClassificationOfficeProject area
April 8, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 13, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 16, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Huzhou Zhanwang Pharmaceutical Co., Ltd.
  • FDA Inspection 966455 - 2016-04-08
  • FDA Inspection 850476 - 2013-09-13
  • FDA Inspection 683244 - 2010-09-16

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