# Iridex Corporation – FDA Inspection, Aug 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/iridex-corporation/e42a6ad6-fa89-4e3c-8e38-bfb36ad7ea6e
Source feed: FDA_Inspections

> FDA inspection 1123978 of Iridex Corporation, August 08, 2019. Form 483 issued. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1123978
- Company Name: Iridex Corporation
- Inspection Date: 2019-08-08
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: San Francisco District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1218928 - 2023-09-20](https://www.keypedia.com/records/fda_inspections/iridex-corporation/e5155730-a969-4724-8442-87294181205d)
- FDA Inspection 1201060 - 2023-03-02
- FDA Inspection 988542 - 2016-08-19
- [FDA Inspection 906286 - 2014-12-02](https://www.keypedia.com/records/fda_inspections/iridex-corporation/d4fe386a-0182-42aa-8531-a7967d863d10)
- [FDA Inspection 836353 - 2013-07-10](https://www.keypedia.com/records/fda_inspections/iridex-corporation/fbbfb6b6-5bf0-4965-9b9e-eceb421c48db)

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

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df