PMDA inspection
Meiji Seika Pharmatech Co., Ltd. Ashigara manufacturing warehouse
PMDA inspection 5130608018147 · Japan · Suitable
Key facts
| Control number | 5130608018147 |
|---|---|
| Manufacturing site | Meiji Seika Pharmatech Co., Ltd. Ashigara manufacturing warehouse |
| Location | 788 Kayayama, Odawara City, Kanagawa Prefecture |
| Country | Japan |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | Remote |
| Inspection month | Jul 1, 2024 |
| Result | Suitable |
| Result notified | Aug 2, 2024 |
| PMDA registration | 14AZ200166 |
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