FDA Inspection 1170726 — Lightera LLC

Lightera LLC — FEI 1221275

The FDA completed an inspection of Lightera LLC on May 23, 2022 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
May 23, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Avon, CT (United States)