PMDA inspection
Nipro Pharma Co., Ltd. Ise Factory
PMDA inspection 5130508034715 · Japan · Suitable
Key facts
| Control number | 5130508034715 |
|---|---|
| Manufacturing site | Nipro Pharma Co., Ltd. Ise Factory |
| Location | 647-240 Ureshino Tenkajicho, Matsusaka City, Mie Prefecture |
| Country | Japan |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | Remote |
| Inspection month | Feb 1, 2024 |
| Result | Suitable |
| Result notified | Mar 6, 2024 |
| PMDA registration | 24AZ000092 |
| FEI numbers | 3013780668 |
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