FDA Inspection 1230383 — MEDAXIS AG

MEDAXIS AG — FEI 3014118821

The FDA completed an inspection of MEDAXIS AG on Jan 31, 2024 in Baar. 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
Jan 31, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Baar (Switzerland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.