FDA Inspection 1030486 — Vitrex Medical A/S
The FDA completed an inspection of Vitrex Medical A/S on June 1, 2017 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
- June 1, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Herlev (Denmark)