FDA Inspection 1036680 — MicroVision, Inc.
The FDA completed an inspection of MicroVision, Inc. on December 6, 2017 in Seabrook, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 6, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Seabrook, NH (United States)