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FDA Inspection
•Zhejiang Jiangbei Pharmaceutical Co., Ltd.•May 6, 2016

Zhejiang Jiangbei Pharmaceutical Co., Ltd. – FDA Inspection, May 6, 2016

Record Details

This FDA Inspection record concerns Zhejiang Jiangbei Pharmaceutical Co., Ltd., with an inspection on May 6, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Jiangbei Pharmaceutical Co., Ltd.
Inspection Date
May 6, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · a56d2196-5178-4bb1-8914-56460d9b5c60

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
973552
FDA center
Human Drugs
Project area
Drug Quality Assurance

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

2
DateClassificationOfficeProject area
July 7, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 3, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Jiangbei Pharmaceutical Co., Ltd.
  • FDA Inspection 1211246 - 2023-07-07
  • FDA Inspection 875391 - 2014-04-03

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