# FDA Inspection 667337 - Cardea Technology, Inc - June 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/cardea-technology-inc/f1a55c7a-15ff-48bb-a57a-eaba3bb04cb9
Source feed: FDA_Inspections

> FDA Inspection 667337 for Cardea Technology, Inc on June 21, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 667337
- Company Name: Cardea Technology, Inc
- Inspection Date: 2010-06-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 721953 - 2011-04-29](https://www.keypedia.com/records/fda_inspections/cardea-technology-inc/f1dd2313-1495-47f3-9f9d-ecaa0570d1a4)

Company: https://www.keypedia.com/companies/cardea-technology-inc/d2089b29-2670-41a4-8409-d94132de1d5c

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