FDA Inspection
Zhejiang Jingwei Pharmaceutical Co., Ltd.Zhejiang Jingwei Pharmaceutical Co., Ltd. – FDA Inspection, Mar 2, 2017
Record Details
This FDA Inspection record concerns Zhejiang Jingwei Pharmaceutical Co., Ltd., with an inspection on March 2, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 0f33300e-9fc8-4879-a89f-c741cc02b21c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1010783
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Jingwei Pharmaceutical Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 22, 2024 | Not classified | Office of Inspections and Investigations | |
| March 15, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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