PMDA inspection
Wyeth Pharmaceutical Division of Wyeth Holdings LLC
PMDA inspection 5130508030331 · USA · Suitable
Key facts
| Control number | 5130508030331 |
|---|---|
| Manufacturing site | Wyeth Pharmaceutical Division of Wyeth Holdings LLC |
| Location | 4300 Oak Park, Sanford, North Carolina 27330, USA |
| Country | USA |
| Product type | Pharmaceuticals |
| Application type | New |
| Inspection method | Remote |
| Inspection month | Feb 1, 2024 |
| Result | Suitable |
| Result notified | Feb 19, 2024 |
| PMDA registration | AG30400192 |
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