# FDA Inspection 846659 - Corgenix, Inc. - August 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/corgenix-inc/0135e296-9532-4b5e-9fed-8c4868dc83dc
Source feed: FDA_Inspections

> FDA Inspection 846659 for Corgenix, Inc. on August 30, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 846659
- Company Name: Corgenix, Inc.
- Inspection Date: 2013-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 846659 - 2013-08-30](https://www.keypedia.com/records/fda_inspections/corgenix-inc/5791f206-8890-4117-a8ae-467f1500ad1a)

Company: https://www.keypedia.com/companies/corgenix-inc/f5bc937e-7d65-4bbf-a44a-a63d7740f62b

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