PMDA inspection
Megafine Pharma(P)Limited Nashik Plant
PMDA inspection 5130508041935 · India · Suitable
Key facts
| Control number | 5130508041935 |
|---|---|
| Manufacturing site | Megafine Pharma(P)Limited Nashik Plant |
| Location | Plot No. 1 to 5, 31 to 35 & 48 to 51, 26 & K/201, Lakhmapur, Tal. Dindori, Dist. Nashik-422 202, Maharashtra, India |
| Country | India |
| Product type | Pharmaceuticals |
| Application type | Regular |
| Inspection method | Remote |
| Inspection month | Mar 1, 2024 |
| Result | Suitable |
| Result notified | Mar 15, 2024 |
| PMDA registration | AG12300130 |
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