FDA Inspection 1069270 — Makeblock Co. Ltd.
The FDA completed an inspection of Makeblock Co. Ltd. on Dec 7, 2017 in Shenzhen. 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 7, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)