Dexcowin Co. Ltd.FDA
- FEI
- 3007065358
- Record date
- Establishment
- Manufacturer
- Location
- Korea
Every published Form FDA 483 issued in February 2023, drawn from the FDA OII FOIA Electronic Reading Room. Each row links to the FDA source record.
6
Published 483s in February 2023
6
Distinct firms
| Company | FEI | Establishment type | Location | FDA date | Source |
|---|---|---|---|---|---|
| Dexcowin Co. Ltd. | 3007065358 | Manufacturer | Korea | FDA | |
| Meridian Made | 3015728839 | Manufacturer | Pennsylvania, United States | FDA | |
| Jubilant HollisterStier General Partnership | 3001623073 | Finished Pharmaceutical Manufacturer | Canada | FDA | |
| AGC Biologics, Inc. | 3000209996 | Human Drug Manufacturer | United States | FDA | |
| Nephron Sterile Compounding Center LLC | 3011158388 | Outsourcing Facility | South Carolina, United States | FDA | |
| Cipla Limited | 3008581988 | Finished Pharmaceutical Manufacturer | United States | FDA |