FDA Inspection
Zhejiang Hisoar Pharmaceutical Co. Ltd.Zhejiang Hisoar Pharmaceutical Co. Ltd. – FDA Inspection, Mar 9, 2018
Record Details
This FDA Inspection record concerns Zhejiang Hisoar Pharmaceutical Co. Ltd., with an inspection on March 9, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d0941bf5-ceb4-4571-b81c-1614c12488b7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1048535
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Hisoar Pharmaceutical Co. Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2015 | OAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| January 18, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 29, 2009 | VAI | Center for Veterinary Medicine | Pre-Approval Eval. of Animal Drugs and Food Additives |
Other documents for Zhejiang Hisoar Pharmaceutical Co. Ltd.
- FDA Inspection 938356 - 2015-08-13
- FDA Inspection 819284 - 2013-01-18
- FDA Inspection 610604 - 2009-08-29
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