FDA Inspection
Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. – FDA Inspection, Sep 26, 2014
Record Details
This FDA Inspection record concerns Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd., with an inspection on September 26, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 26, 2014
- Product Type
- Drugs
View Company Profile
ID · fac862ec-bc15-4d64-bb27-404bd549af18
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 898136
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
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 | |
| September 20, 2019 | 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 |
Other documents for Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.
- FDA Inspection 1294476 - 2025-10-31
- FDA Inspection 1107473 - 2019-09-20
- FDA Inspection 1037415 - 2017-11-02
- FDA Inspection 980719 - 2016-07-08
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