FDA Inspection 583444 — LightVision Technologies Corp
The FDA completed an inspection of LightVision Technologies Corp on Apr 9, 2009 in Taoyuan. 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
- Apr 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Taoyuan (Taiwan)