FDA Inspection
Zhejiang Cheng Yi Pharmaceutical Co., Ltd.Zhejiang Cheng Yi Pharmaceutical Co., Ltd. – FDA Inspection, Mar 7, 2025
Record Details
This FDA Inspection record concerns Zhejiang Cheng Yi Pharmaceutical Co., Ltd., with an inspection on March 7, 2025, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- March 7, 2025
- Product Type
- Human Drugs
View Company Profile
ID · 7a6c43ae-236c-4cbb-b540-57813800fccc
Inspection Facts
- Inspection number
- 1265837
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 22, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 15, 2016 | 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 1111465 - 2019-11-22
- FDA Inspection 985172 - 2016-07-15
- FDA Inspection 879798 - 2014-03-14
- FDA Inspection 701018 - 2010-09-09
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