FDA Inspection 1089557 — Beijing E-Plus 3D Technology Co. Ltd.
The FDA completed an inspection of Beijing E-Plus 3D Technology Co. Ltd. on Nov 8, 2018 in Changping. 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 8, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Changping (China)