FDA Inspection 927834 — Belimed AG

Belimed AG — FEI 3003927243

The FDA completed an inspection of Belimed AG on Apr 16, 2015 in Sulgen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 16, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sulgen (Switzerland)