PMDA inspection
Shandong Anxin Pharmaceutical Co., Ltd.
PMDA inspection 5130508015930 · China · Suitable
Key facts
| Control number | 5130508015930 |
|---|---|
| Manufacturing site | Shandong Anxin Pharmaceutical Co., Ltd. |
| Location | No.849 Dongjia Town, Licheng District, Jinan, Shandong Province, P.R.CHINA |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | On-Site |
| Inspection month | Dec 1, 2023 |
| Result | Suitable |
| Result notified | Mar 15, 2024 |
| PMDA registration | AG10500200 |
| FEI numbers | 3004229375 |
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