PMDA inspection
Lianhe Aigen Pharma Co., Ltd.
PMDA inspection 5130508035703 · China · Suitable
Key facts
| Control number | 5130508035703 |
|---|---|
| Manufacturing site | Lianhe Aigen Pharma Co., Ltd. |
| Location | No. 3 Donghai 8th Avenue, Toumengang New District, Taizhou, Zhejiang 317016, China (CHN) |
| Country | China |
| Product type | Pharmaceuticals |
| Application type | New |
| Inspection method | Remote |
| Inspection month | May 1, 2024 |
| Result | Suitable |
| Result notified | May 23, 2024 |
| PMDA registration | AG10500722 |
| FEI numbers | 3012828549 |
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