PMDA inspection
Zhejiang Liaoyuan Pharmaceutical Co., Ltd.
PMDA inspection 5130508015219 · China · Suitable
Key facts
| Control number | 5130508015219 |
|---|---|
| Manufacturing site | Zhejiang Liaoyuan Pharmaceutical Co., Ltd. |
| Location | Zhejiang Provincial Chemical and Medical Raw Material Base Linhai Zone Duqiao town, Linhai City, Zhejiang Province, China |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | On-Site |
| Inspection month | Mar 1, 2024 |
| Result | Suitable |
| Result notified | Jul 19, 2024 |
| PMDA registration | AG10500132 |
| FEI numbers | 3007388805 |
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