FDA Inspection 1298668 — Maxxos-Medical Gmbh

Maxxos-Medical Gmbh — FEI 3011354099

The FDA completed an inspection of Maxxos-Medical Gmbh on Dec 17, 2025 in Mahlstetten. 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
Dec 17, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mahlstetten (Germany)

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