FDA Inspection 1238904 — Medistri SA

Medistri SA — FEI 3006946276

The FDA completed an inspection of Medistri SA on May 9, 2024 in Domdidier. 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
May 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Domdidier (Switzerland)