FDA Inspection 913515 — MicroVision, Inc.

MicroVision, Inc. — FEI 3002532015

The FDA completed an inspection of MicroVision, Inc. on January 22, 2015 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
January 22, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Seabrook, NH (United States)