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FDA Inspection
•Zhejiang Huahai Pharmaceutical Co., Ltd.•March 27, 2015

Zhejiang Huahai Pharmaceutical Co., Ltd. – FDA Inspection, Mar 27, 2015

Record Details

This FDA Inspection record concerns Zhejiang Huahai Pharmaceutical Co., Ltd., with an inspection on March 27, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Huahai Pharmaceutical Co., Ltd.
Inspection Date
March 27, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 98610561-1547-4923-aaf6-de97c6883bb5

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
921574
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Huahai Pharmaceutical Co., Ltd.

10
DateClassificationOfficeProject area
April 24, 2026Not classifiedOffice of Inspections and Investigations
January 24, 2025OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 2, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 28, 2019Not classifiedOffice of Inspections and Investigations
May 31, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 10 other inspections on the company page
Other documents for Zhejiang Huahai Pharmaceutical Co., Ltd.
  • FDA Inspection 1319736 - 2026-04-24
  • FDA Inspection 1259818 - 2025-01-24
  • FDA Inspection 1149252 - 2021-07-02
  • FDA Inspection 1094941 - 2019-06-28
  • FDA Inspection 1093250 - 2019-05-31

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