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FDA Inspection
•Zhejiang Haizhou Pharmaceutical Co., Ltd.•August 7, 2014

Zhejiang Haizhou Pharmaceutical Co., Ltd. – FDA Inspection, Aug 7, 2014

Record Details

This FDA Inspection record concerns Zhejiang Haizhou Pharmaceutical Co., Ltd., with an inspection on August 7, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Haizhou Pharmaceutical Co., Ltd.
Inspection Date
August 7, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · bede4e3b-cfb5-4a1a-9a17-f1dccd085ac7

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
893991
FDA center
Human Drugs
Project area
Drug Quality Assurance

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

3
DateClassificationOfficeProject area
April 18, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 18, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Haizhou Pharmaceutical Co., Ltd.
  • FDA Inspection 1271224 - 2025-04-18
  • FDA Inspection 1078048 - 2019-01-18
  • FDA Inspection 742581 - 2011-06-30

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