FDA Inspection 955461 — Shenzhen Supernova Laser Equipment Co Ltd
The FDA completed an inspection of Shenzhen Supernova Laser Equipment Co Ltd on December 11, 2015 in Shenzhen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- December 11, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)