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