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FDA Inspection
•Zhejiang Jingwei Pharmaceutical Co., Ltd.•March 15, 2019

Zhejiang Jingwei Pharmaceutical Co., Ltd. – FDA Inspection, Mar 15, 2019

Record Details

This FDA Inspection record concerns Zhejiang Jingwei Pharmaceutical Co., Ltd., with an inspection on March 15, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Jingwei Pharmaceutical Co., Ltd.
Inspection Date
March 15, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Michele Perry-Williams (FDA Associated Person)
View Company Profile

ID · d77438d5-afeb-412d-9c55-24d797529e53

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1086689
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

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

2
DateClassificationOfficeProject area
November 22, 2024Not classifiedOffice of Inspections and Investigations
March 2, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Jingwei Pharmaceutical Co., Ltd.
  • FDA Inspection 1255518 - 2024-11-22
  • FDA Inspection 1010783 - 2017-03-02

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