FDA Inspection 1295680 — Radiometer Minneapolis
The FDA completed an inspection of Radiometer Minneapolis on Dec 4, 2025 in New Brighton, MN. 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
- Dec 4, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Brighton, MN (United States)