FDA Inspection 1246455 — Medartis AG

Medartis AG — FEI 3003236702

The FDA completed an inspection of Medartis AG on Jul 15, 2024 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 15, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Basel Town (Switzerland)