FDA Inspection 620307 — CG MedTech Co. Ltd
The FDA completed an inspection of CG MedTech Co. Ltd on September 25, 2009 in Seongnam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 25, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Seongnam (Korea (the Republic of))