# Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd., Taizhou, China – FDA Inspections

Source: https://www.keypedia.com/companies/zhejiang-hisoar-chuannan-pharmaceutical-co-ltd/49f209c0-5102-42ad-b7ce-27529f15c6a5

> Inspection records and compliance data for Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. in Taizhou. 5 FDA inspections on record, 1 Form 483, last inspected October 31, 2025.

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## Details

- Name: Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd.
- FEI Number: 3006545436
- Business Operations: API MANUFACTURE
- Address Line 1: No. 23 5th Donghai Ave., Zhejiang Chemical Materials Base Linhai Zone
- City: Taizhou
- Country Name: China
- Address: No. 23 5th Donghai Ave., Zhejiang Chemical Materials Base Linhai Zone, Taizhou, China
- Country: China

## Related Documents

- FDA Inspection 1294476 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2025-10-31 — source: FDA, date: October 31, 2025
- FDA Inspection 1294476 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2025-10-31 — source: FDA, date: October 31, 2025
- FDA Inspection 1294476 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2025-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2025
- FDA Inspection 1294476 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2025-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2025
- [483 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2019-09-20](https://www.keypedia.com/records/483/zhejiang-hisoar-chuannan-pharmaceutical-co-ltd/821da991-13b4-4894-ada1-9ef1ab13f09a) — source: FDA, date: September 20, 2019
- [FDA Inspection 1107473 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2019-09-20](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-chuannan-pharmaceutical-co-ltd/cbfdba07-62dd-410a-b272-149016d519eb) — source: FDA, date: September 20, 2019
- FDA Inspection 1037415 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2017-11-02 — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2017
- FDA Inspection 980719 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2016-07-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 8, 2016
- FDA Inspection 980719 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2016-07-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 8, 2016
- [FDA Inspection 898136 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2014-09-26](https://www.keypedia.com/records/fda_inspections/zhejiang-hisoar-chuannan-pharmaceutical-co-ltd/fac862ec-bc15-4d64-bb27-404bd549af18) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2014
- FDA Inspection 898136 - Zhejiang Hisoar Chuannan Pharmaceutical Co. Ltd. - 2014-09-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2014

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