FDA Inspection 1058088 — Guangzhou Hymson Laser Technology Co. Ltd.
The FDA completed an inspection of Guangzhou Hymson Laser Technology Co. Ltd. on Nov 30, 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
- Nov 30, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Guangzhou (China)