FDA Inspection 1237139 — NORLASE APS
The FDA completed an inspection of NORLASE APS on Mar 21, 2024 in Ballerup. 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
- Mar 21, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ballerup (Denmark)