# FDA Inspection 836353 - Iridex Corporation - July 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/iridex-corporation/fbbfb6b6-5bf0-4965-9b9e-eceb421c48db
Source feed: FDA_Inspections

> FDA Inspection 836353 for Iridex Corporation on July 10, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 836353
- Company Name: Iridex Corporation
- Inspection Date: 2013-07-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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