PMDA inspection
Taiho Pharmaceutical Co., Ltd. Saitama Factory
PMDA inspection 5130608019013 · Japan · Suitable
Key facts
| Control number | 5130608019013 |
|---|---|
| Manufacturing site | Taiho Pharmaceutical Co., Ltd. Saitama Factory |
| Location | 200-22 Motohara, Kamikawa-cho, Kodama-gun, Saitama Prefecture |
| Country | Japan |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | Remote |
| Inspection month | Oct 1, 2024 |
| Result | Suitable |
| Result notified | Oct 15, 2024 |
| PMDA registration | 11AZ005003 |
| FEI numbers | 3002646390 |
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