# FDA Inspection 1218928 - Iridex Corporation - September 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/iridex-corporation/4bdb2a3b-5fc6-411f-8277-3bf854b018ce
Source feed: FDA_Inspections

> FDA Inspection 1218928 for Iridex Corporation on September 20, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1218928
- Company Name: Iridex Corporation
- Inspection Date: 2023-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1218928 - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/e5155730-a969-4724-8442-87294181205d)
- [FDA Inspection 1218928 - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/9aa22912-7388-4d1d-87e0-4c30243bb5c1)
- [FDA Inspection 988542 - 2016-08-19](https://www.keypedia.com/records/fda_inspections/iridex-corporation/41d551ea-d637-4570-8a39-a1e566918f81)
- [FDA Inspection 988542 - 2016-08-19](https://www.keypedia.com/records/fda_inspections/iridex-corporation/019de454-0f88-4c63-bf9d-b3a02a6b5770)
- [FDA Inspection 906286 - 2014-12-02](https://www.keypedia.com/records/fda_inspections/iridex-corporation/d4fe386a-0182-42aa-8531-a7967d863d10)

Company: https://www.keypedia.com/companies/iridex-corporation/9c886e2b-8873-4b61-b8b2-468461ced7a5

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