# FDA Inspection 923120 - Eyegaze Inc. - April 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/eyegaze-inc/bfaa24ef-421b-4d92-8bfb-85202596cf8f
Source feed: FDA_Inspections

> FDA Inspection 923120 for Eyegaze Inc. on April 23, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 923120
- Company Name: Eyegaze Inc.
- Inspection Date: 2015-04-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1268684 - 2025-05-02](https://www.keypedia.com/records/fda_inspections/eyegaze-inc/229a9afe-51b4-4cb5-be0d-23a8eb4b1b46)
- [FDA Inspection 1268684 - 2025-05-02](https://www.keypedia.com/records/fda_inspections/eyegaze-inc/714dd473-e479-4970-a398-09d169f89f41)
- [FDA Inspection 1268684 - 2025-05-02](https://www.keypedia.com/records/fda_inspections/eyegaze-inc/de2699d5-96ee-4cbb-ad4f-b2f2863800e7)
- [FDA Inspection 1268684 - 2025-05-02](https://www.keypedia.com/records/fda_inspections/eyegaze-inc/c962edc8-bffc-4cfa-9e30-f75e7a04d5e4)
- [FDA Inspection 1153994 - 2021-10-08](https://www.keypedia.com/records/fda_inspections/eyegaze-inc/3e83a5d3-73a2-4e8e-8c19-de2246cb699b)

Company: https://www.keypedia.com/companies/eyegaze-inc/b7226d9c-3955-4414-9eaa-53fe6e780b31

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