FDA Inspection 1256406 — Lightera LLC
The FDA completed an inspection of Lightera LLC on Nov 7, 2024 in Avon, 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
- Nov 7, 2024
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Avon, CT (United States)