FDA Inspection 1017808 — Radiometer Medical ApS

Radiometer Medical ApS — FEI 3002807968

The FDA completed an inspection of Radiometer Medical ApS on May 11, 2017 in Bronshoj. 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 11, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bronshoj (Denmark)