FDA Inspection
Zhejiang Cheng Yi Pharmaceutical Co., Ltd.Zhejiang Cheng Yi Pharmaceutical Co., Ltd. – FDA Inspection, Jul 15, 2016
Record Details
This FDA Inspection record concerns Zhejiang Cheng Yi Pharmaceutical Co., Ltd., with an inspection on July 15, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 15, 2016
- Product Type
- Drugs
View Company Profile
ID · 3fc13e2e-a088-41d6-8d9d-1aa9ff21a885
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 985172
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 7, 2025 | Not classified | Office of Inspections and Investigations | |
| November 22, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 14, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 9, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
- FDA Inspection 1265837 - 2025-03-07
- FDA Inspection 1111465 - 2019-11-22
- FDA Inspection 879798 - 2014-03-14
- FDA Inspection 701018 - 2010-09-09
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