PMDA inspection
KBI Biopharma, Inc. (Boulder)
PMDA inspection 5130608038352 · USA · Suitable
Key facts
| Control number | 5130608038352 |
|---|---|
| Manufacturing site | KBI Biopharma, Inc. (Boulder) |
| Location | 2500 Central Ave., Boulder, Colorado (CO) 80301, United States (USA) |
| Country | USA |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | Remote |
| Inspection month | Feb 1, 2025 |
| Result | Suitable |
| Result notified | Mar 3, 2025 |
| PMDA registration | AG30400626 |
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