# FDA Inspection 971843 - Cardia Inc - May 02, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/cardia-inc/ff780d41-0458-4597-be39-4813b78ed5e0/
Source feed: FDA_Inspections

> FDA Inspection 971843 for Cardia Inc on May 02, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971843
- Company Name: Cardia Inc
- Inspection Date: 2016-05-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 813176 - 2012-12-19](https://www.globalkeysolutions.net/api/records/fda_inspections/cardia-inc/60d5f3b8-d9a1-4a7f-ae30-e7a6d6998a7b/)
- [FDA Inspection 726443 - 2011-05-18](https://www.globalkeysolutions.net/api/records/fda_inspections/cardia-inc/f7d24380-f2cd-412b-9708-cd8327ef7ddd/)

Company: https://www.globalkeysolutions.net/companies/cardia-inc/76daf619-6add-4924-b87b-904e84b8e285

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