FDA Inspection 1241138 — Unomedical A/S

Unomedical A/S — FEI 1000477110

The FDA completed an inspection of Unomedical A/S on May 24, 2024 in Lejre. 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 24, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Lejre (Denmark)