FDA Inspection 1069974 — SOMNOmedics AG

SOMNOmedics AG — FEI 3006258337

The FDA completed an inspection of SOMNOmedics AG on Sep 13, 2018 in Randersacker. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Randersacker (Germany)