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 VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 17, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Brea, CA (United States)