# FDA Inspection 854394 - Cardiox Corporation - October 30, 2013

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

> FDA Inspection 854394 for Cardiox Corporation on October 30, 2013. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 954371 - 2015-12-18](https://www.globalkeysolutions.net/records/fda_inspections/cardiox-corporation/de1950ce-92b8-489b-b69d-8d1b0459c94c)
- [FDA Inspection 954371 - 2015-12-18](https://www.globalkeysolutions.net/records/fda_inspections/cardiox-corporation/fbdbbc38-d47f-4f1c-a5fc-8df25191946f)
- [FDA Inspection 854394 - 2013-10-30](https://www.globalkeysolutions.net/records/fda_inspections/cardiox-corporation/2b029d90-74e1-417e-b290-1296d6df2d76)

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

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