FDA Inspection
Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API).Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API). – FDA Inspection, Jul 20, 2023
Record Details
This FDA Inspection record concerns Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API)., with an inspection on July 20, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 20, 2023
- Product Type
- Drugs
View Company Profile
ID · 59fa6bce-3222-43c8-b35c-4563acd3e8e4
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1214801
- 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 |
|---|---|---|---|
| August 23, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 1, 2014 | NAI | 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 1101264 - 2019-08-23
- FDA Inspection 893334 - 2014-08-01
- FDA Inspection 738535 - 2011-07-21
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.