FDA Inspection 732009 — Dexcowin Co. Ltd.
The FDA completed an inspection of Dexcowin Co. Ltd. on Jun 3, 2011 in Geumcheon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 3, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Geumcheon (Korea (the Republic of))