FDA Inspection
Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. – FDA Inspection, Sep 20, 2019
Record Details
This FDA Inspection record concerns Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd., with an inspection on September 20, 2019, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- September 20, 2019
- Product Type
- Human Drugs
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ID · cbfdba07-62dd-410a-b272-149016d519eb
Inspection Facts
- Inspection number
- 1107473
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2025 | Not classified | Office of Inspections and Investigations | |
| November 2, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 8, 2016 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| September 26, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.
- FDA Inspection 1294476 - 2025-10-31
- FDA Inspection 1037415 - 2017-11-02
- FDA Inspection 980719 - 2016-07-08
- FDA Inspection 898136 - 2014-09-26
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