PMDA inspection
Meiji Seika Pharmatech Co., Ltd.
PMDA inspection 5130608028177 · Japan · Suitable
Key facts
| Control number | 5130608028177 |
|---|---|
| Manufacturing site | Meiji Seika Pharmatech Co., Ltd. |
| Location | 1056 Kamomiya, Odawara City, Kanagawa Prefecture |
| Country | Japan |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | On-Site |
| Inspection month | Sep 1, 2024 |
| Result | Suitable |
| Result notified | Jan 27, 2025 |
| PMDA registration | 14AZ100009 |
| FEI numbers | 3015407855 |
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