FDA Inspection 1026160 — MedAire, Inc.

MedAire, Inc. — FEI 3005798963

The FDA completed an inspection of MedAire, Inc. on May 12, 2017 in Phoenix, AZ. 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
May 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)