FDA Inspection 922594 — CG MedTech Co., Ltd.
The FDA completed an inspection of CG MedTech Co., Ltd. on Feb 5, 2015 in Uijeongbu. 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
- Feb 5, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Uijeongbu (Korea (the Republic of))
Additional details
Postmarket Audit Inspections