FDA Inspection 1101394 — Belimed AG

Belimed AG — FEI 3001061128

The FDA completed an inspection of Belimed AG on June 19, 2019 in Zug. 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
June 19, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Zug (Switzerland)