FDA Inspection 940243 — Medartis AG

Medartis AG — FEI 3003236702

The FDA completed an inspection of Medartis AG on Jul 30, 2015 in Basel Town. 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
Jul 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Basel Town (Switzerland)