# Zhejiang Jingwei Pharmaceutical Co., Ltd. – FDA Inspection, Mar 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/zhejiang-jingwei-pharmaceutical-co-ltd/0f33300e-9fc8-4879-a89f-c741cc02b21c
Source feed: FDA_Inspections

> FDA inspection 1010783 of Zhejiang Jingwei Pharmaceutical Co., Ltd., March 02, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010783
- Company Name: Zhejiang Jingwei Pharmaceutical Co., Ltd.
- Inspection Date: 2017-03-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/matthew-b-casale/e78481c6-5fbd-4723-a79c-167176395af8)

Company: https://www.keypedia.com/companies/zhejiang-jingwei-pharmaceutical-co-ltd/f8f377b7-d943-41e1-b510-f712bcfd68ed

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c