# Iridex Corporation - Inspection Records

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

> Inspection records and compliance data for Iridex Corporation in Mountain View, California. Access full analysis and detailed observations.

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## Details

- Name: Iridex Corporation
- FEI Number: 2939653
- City: Mountain View
- State: California
- Country Name: United States
- Address Line 1: 1212 Terra Bella Ave
- Zip Code: 94043

## Related Documents

- [483 - Iridex Corporation - 2023-09-20](https://www.keypedia.com/records/483/iridex-corporation/5f3ce6cb-7506-49da-926e-f68ba7eff6c6) — source: FDA, date: September 20, 2023
- [483 - Iridex Corporation - 2023-09-20](https://www.keypedia.com/records/483/iridex-corporation/993847e9-01f7-4291-8824-6b96a87b028d) — source: FDA, date: September 20, 2023
- [FDA Inspection 1218928 - Iridex Corporation - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/e5155730-a969-4724-8442-87294181205d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 20, 2023
- [FDA Inspection 1218928 - Iridex Corporation - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/9aa22912-7388-4d1d-87e0-4c30243bb5c1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 20, 2023
- [FDA Inspection 1218928 - Iridex Corporation - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/4bdb2a3b-5fc6-411f-8277-3bf854b018ce) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2023
- [FDA Inspection 1201060 - Iridex Corporation - 2023-03-02](https://www.keypedia.com/records/fda_inspections/iridex-corporation/90917172-4af8-45d5-90c9-92c14a7b9d2c) — source: FDA, date: March 2, 2023
- [FDA Inspection 988542 - Iridex Corporation - 2016-08-19](https://www.keypedia.com/records/fda_inspections/iridex-corporation/019de454-0f88-4c63-bf9d-b3a02a6b5770) — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2016
- [FDA Inspection 988542 - Iridex Corporation - 2016-08-19](https://www.keypedia.com/records/fda_inspections/iridex-corporation/41d551ea-d637-4570-8a39-a1e566918f81) — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2016
- [FDA Inspection 906286 - Iridex Corporation - 2014-12-02](https://www.keypedia.com/records/fda_inspections/iridex-corporation/d4fe386a-0182-42aa-8531-a7967d863d10) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 2, 2014
- [FDA Inspection 906286 - Iridex Corporation - 2014-12-02](https://www.keypedia.com/records/fda_inspections/iridex-corporation/3b4ac1af-7d2d-407b-aa5c-50d249a4c9e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 2, 2014
- [FDA Inspection 836353 - Iridex Corporation - 2013-07-10](https://www.keypedia.com/records/fda_inspections/iridex-corporation/89d25b77-81dd-42bc-9330-dd7c109cf0b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2013
- [FDA Inspection 836353 - Iridex Corporation - 2013-07-10](https://www.keypedia.com/records/fda_inspections/iridex-corporation/fbbfb6b6-5bf0-4965-9b9e-eceb421c48db) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2013

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