PMDA inspection
Zhejiang Hisoar Chuannan Pharmaceutical Co., Ltd.
PMDA inspection 5130508019817 · China · Suitable
Key facts
| Control number | 5130508019817 |
|---|---|
| Manufacturing site | Zhejiang Hisoar Chuannan Pharmaceutical Co., Ltd. |
| Location | No.23, 5th Donghai Avenue Zhejiang Chemical materials base Linhai zone, Linhai city, Zhejiang Province, China. |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | On-Site |
| Inspection month | Aug 1, 2024 |
| Result | Suitable |
| Result notified | Oct 31, 2025 |
| PMDA registration | AG10500392 |
| FEI numbers | 3006545436 |
About PMDA GMP inspections (Japan)
Japan's PMDA conducts GMP and QMS inspections of domestic and foreign manufacturing sites that supply the Japanese market.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan