FDA Inspection 1342880 — Lumendi, LLC
The FDA completed an inspection of Lumendi, LLC on Oct 21, 2026 in Westport, CT. 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
- Oct 21, 2026
- Fiscal Year
- 2027
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Westport, CT (United States)