PMDA inspection
Mylan Laboratories Limited (Formulation)
PMDA inspection 5130708010870 · India · Suitable
Key facts
| Control number | 5130708010870 |
|---|---|
| Manufacturing site | Mylan Laboratories Limited (Formulation) |
| Location | F-4 & F-12, Malegaon MIDC, Sinnar, Nashik-422 113, Maharashtra, India |
| Country | India |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | Remote |
| Inspection month | Apr 1, 2025 |
| Result | Suitable |
| Result notified | May 14, 2025 |
| PMDA registration | AG12300175 |
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