FDA Inspection 942750 — POINTIMPLANT CO., LTD.
The FDA completed an inspection of POINTIMPLANT CO., LTD. on Sep 22, 2015 in Gwangmyeong. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Gwangmyeong (Korea (the Republic of))