# Cardiox Corporation – FDA Inspection, Oct 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/cardiox-corporation/4f0b10ef-5520-4fd7-8274-208075a83c8f
Source feed: FDA_Inspections

> FDA inspection 854394 of Cardiox Corporation, October 30, 2013. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 854394
- Company Name: Cardiox Corporation
- Inspection Date: 2013-10-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 954371 - 2015-12-18](https://www.keypedia.com/records/fda_inspections/cardiox-corporation/fbdbbc38-d47f-4f1c-a5fc-8df25191946f)

Company: https://www.keypedia.com/companies/cardiox-corporation/8ca18abc-ab04-451a-934e-6f78514214ed

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