FDA Inspection 1302726 — Rejoni, Inc.
The FDA completed an inspection of Rejoni, Inc. on Feb 9, 2026 in Bedford, MA. 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
- Feb 9, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Bedford, MA (United States)