FDA Inspection
Zhejiang Charioteer Pharmaceutical Co. Ltd.Zhejiang Charioteer Pharmaceutical Co. Ltd. – FDA Inspection, Nov 8, 2024
Record Details
This FDA Inspection record concerns Zhejiang Charioteer Pharmaceutical Co. Ltd., with an inspection on November 8, 2024, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- November 8, 2024
- Product Type
- Human Drugs
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ID · e0d27ae0-7151-4fe3-93e7-497d4ac61191
Inspection Facts
- Inspection number
- 1257164
- FDA center
- Human Drugs
Other FDA inspections of Zhejiang Charioteer Pharmaceutical Co. Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 12, 2026 | Not classified | Office of Inspections and Investigations | |
| January 18, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 4, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 15, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Charioteer Pharmaceutical Co. Ltd.
- FDA Inspection 1328192 - 2026-06-12
- FDA Inspection 1039806 - 2018-01-18
- FDA Inspection 890582 - 2014-07-04
- FDA Inspection 748165 - 2011-09-15
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