FDA Inspection 1252014 — Vitrex Medical A/S

Vitrex Medical A/S — FEI 3003208740

The FDA completed an inspection of Vitrex Medical A/S on September 12, 2024 in Herlev. 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
September 12, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Herlev (Denmark)