FDA Inspection 1277491 — Earlens Corporation

Earlens Corporation — FEI 3010863048

The FDA completed an inspection of Earlens Corporation on July 10, 2025 in Menlo Park, CA. 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
July 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Menlo Park, CA (United States)