FDA Inspection
Zhejiang Hisun Pharmaceutical Co., Ltd.Zhejiang Hisun Pharmaceutical Co., Ltd. – FDA Inspection, Sep 3, 2010
Record Details
This FDA Inspection record concerns Zhejiang Hisun Pharmaceutical Co., Ltd., with an inspection on September 3, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 3, 2010
- Product Type
- Drugs
View Company Profile
ID · 3d85d1b6-9b59-4e45-9d02-257e7206b413
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 694553
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Zhejiang Hisun Pharmaceutical Co., Ltd.
11| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 7, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 11, 2017 | VAI | Center for Veterinary Medicine | Pre-Approval Eval. of Animal Drugs and Food Additives |
| January 19, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 7, 2015 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Hisun Pharmaceutical Co., Ltd.
- FDA Inspection 1238621 - 2024-06-21
- FDA Inspection 1096299 - 2019-06-07
- FDA Inspection 1027076 - 2017-08-11
- FDA Inspection 998186 - 2017-01-19
- FDA Inspection 918008 - 2015-03-07
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