PMDA inspection
Dijia Pharmaceutical Group Co., Ltd.
PMDA inspection 5130508007780 · China · Suitable
Key facts
| Control number | 5130508007780 |
|---|---|
| Manufacturing site | Dijia Pharmaceutical Group Co., Ltd. |
| Location | No.268 Tianrun Road, Wendeng Economic Development Zone, Weihai, Shandong, China |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | Remote |
| Inspection month | Dec 1, 2023 |
| Result | Suitable |
| Result notified | Jan 5, 2024 |
| PMDA registration | AG10500561 |
| FEI numbers | 3011998304 |
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