FDA Inspection
Zhejiang Liaoyuan Pharmaceutical Co., Ltd.Zhejiang Liaoyuan Pharmaceutical Co., Ltd. – FDA Inspection, Jun 9, 2017
Record Details
This FDA Inspection record concerns Zhejiang Liaoyuan Pharmaceutical Co., Ltd., with an inspection on June 9, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 9755a0a7-acdb-40c0-92a1-b296912c46cc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019163
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Liaoyuan Pharmaceutical Co., Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 25, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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