PMDA inspection
Teika Pharmaceutical Co., Ltd. Shinjo Factory
PMDA inspection 5130608024343 · Japan · Suitable
Key facts
| Control number | 5130608024343 |
|---|---|
| Manufacturing site | Teika Pharmaceutical Co., Ltd. Shinjo Factory |
| Location | 1-3-27 Arakawa, Toyama City, Toyama Prefecture |
| Country | Japan |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | Remote |
| Inspection month | Oct 1, 2024 |
| Result | Suitable |
| Result notified | Oct 15, 2024 |
| PMDA registration | 16AZ000001 |
| FEI numbers | 3008982037 |
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