FDA Inspection 1273889 — Medikomp Gmbh

Medikomp Gmbh — FEI 3007427881

The FDA completed an inspection of Medikomp Gmbh on May 14, 2025 in Rastatt. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Rastatt (Germany)