FDA Inspection
Zhejiang Charioteer Pharmaceutical Co. Ltd.Zhejiang Charioteer Pharmaceutical Co. Ltd. – FDA Inspection, Jan 18, 2018
Record Details
This FDA Inspection record concerns Zhejiang Charioteer Pharmaceutical Co. Ltd., with an inspection on January 18, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ec2a6fa6-a3a1-4dae-864e-a2819e03ec39
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1039806
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
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 | |
| November 8, 2024 | Not classified | Office of Inspections and Investigations | |
| 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 1257164 - 2024-11-08
- FDA Inspection 890582 - 2014-07-04
- FDA Inspection 748165 - 2011-09-15
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