PMDA inspection
Zhejiang Changhai Pharmaceuticals Co., Ltd.
PMDA inspection 5130608030192 · China · Suitable
Key facts
| Control number | 5130608030192 |
|---|---|
| Manufacturing site | Zhejiang Changhai Pharmaceuticals Co., Ltd. |
| Location | 188 Mid Zhiyuan Avenue, Binhai New Area, Shaoxing City, Zhejiang, 312366, P.R.China |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | On-Site |
| Inspection month | Aug 1, 2025 |
| Result | Suitable |
| Result notified | Dec 26, 2025 |
| PMDA registration | AG10500643 |
| FEI numbers | 3013591876 |
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