# FDA Inspection 1277491 - Earlens Corporation - July 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/earlens-corporation/56e947f8-fd7c-4dcf-a0d8-d4bf9aef19cd
Source feed: FDA_Inspections

> FDA Inspection 1277491 for Earlens Corporation on July 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1277491
- Company Name: Earlens Corporation
- Inspection Date: 2025-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1277491 - 2025-07-10](https://www.keypedia.com/records/fda_inspections/earlens-corporation/2c6c95d3-3595-45d4-9e05-21d5b3ab2172)
- [FDA Inspection 1277491 - 2025-07-10](https://www.keypedia.com/records/fda_inspections/earlens-corporation/803bce57-20af-4e24-b5ca-b616a3aca522)

Company: https://www.keypedia.com/companies/earlens-corporation/ec2525ff-c22a-494a-ba00-5b11d1ac3b33

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7