PMDA inspection
Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
PMDA inspection 5130508035242 · USA · Suitable
Key facts
| Control number | 5130508035242 |
|---|---|
| Manufacturing site | Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC |
| Location | 1 Burtt Road, Andover, Massachusetts 01810, USA |
| Country | USA |
| Product type | Pharmaceuticals |
| Application type | New |
| Inspection method | Remote |
| Inspection month | May 1, 2024 |
| Result | Suitable |
| Result notified | May 20, 2024 |
| PMDA registration | AG30400437 |
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