PMDA inspection
Cytovance Biologics, Inc.
PMDA inspection 5130708021983 · USA · Suitable
Key facts
| Control number | 5130708021983 |
|---|---|
| Manufacturing site | Cytovance Biologics, Inc. |
| Location | 800/840/885 Research Parkway, Suite 200 Oklahoma City, OK 73104, USA |
| Country | USA |
| Product type | Pharmaceuticals |
| Application type | New |
| Inspection method | Remote |
| Inspection month | Dec 1, 2025 |
| Result | Suitable |
| Result notified | Dec 4, 2025 |
| PMDA registration | AG30400771 |
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