PMDA inspection
Dr.Reddy's Laboratories Ltd. FTO-VII
PMDA inspection 5130608015086 · India · Suitable
Key facts
| Control number | 5130608015086 |
|---|---|
| Manufacturing site | Dr.Reddy's Laboratories Ltd. FTO-VII |
| Location | Plot No. P1 to P9.Phase-III.Duvvada, VSEZ, Visakhapatnam, Andhra Pradesh 530 046, India |
| Country | India |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | Remote |
| Inspection month | Oct 1, 2024 |
| Result | Suitable |
| Result notified | Nov 5, 2024 |
| PMDA registration | AG12300276 |
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