FDA Inspection
Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API).Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API). – FDA Inspection, Aug 1, 2014
Record Details
This FDA Inspection record concerns Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API)., with an inspection on August 1, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 1, 2014
- Product Type
- Drugs
View Company Profile
ID · f3782830-4751-4281-819b-a0f7df73080d
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 893334
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API).
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 20, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 23, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 21, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API).
- FDA Inspection 1214801 - 2023-07-20
- FDA Inspection 1101264 - 2019-08-23
- FDA Inspection 738535 - 2011-07-21
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