FDA Inspection 1089422 — Beijing Sundor Laser Equipment Co. Ltd.
The FDA completed an inspection of Beijing Sundor Laser Equipment Co. Ltd. on Nov 9, 2018 in Beijing. 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 9, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Beijing (China)