FDA Inspection 1025096 — SHENZHEN SUNSHINE LASER DEVICES
The FDA completed an inspection of SHENZHEN SUNSHINE LASER DEVICES on June 2, 2017 in Shenzhen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 2, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)