FDA Inspection 848894 — Medrange Corporation

Medrange Corporation — FEI 3008786200

The FDA completed an inspection of Medrange Corporation on September 17, 2013 in Brea, CA. 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
September 17, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brea, CA (United States)