FDA Inspection 1046760 — Guangzhou Sunine Laser Technology Co. Ltd.
The FDA completed an inspection of Guangzhou Sunine Laser Technology Co. Ltd. on Dec 1, 2017 in Guangzhou. 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
- Dec 1, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Guangzhou (China)