# FDA Inspection 1216854 - Cardionics, Inc - August 30, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/cardionics-inc/1ffabc5d-a823-4987-98e6-55e755382f30
Source feed: FDA_Inspections

> FDA Inspection 1216854 for Cardionics, Inc on August 30, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216854
- Company Name: Cardionics, Inc
- Inspection Date: 2023-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1216854 - 2023-08-30](https://www.globalkeysolutions.net/records/fda_inspections/cardionics-inc/938ddcbc-99cc-4609-af19-7a55d05a658f)
- [FDA Inspection 672698 - 2010-07-23](https://www.globalkeysolutions.net/records/fda_inspections/cardionics-inc/f8e5e157-0910-476a-bb0e-31aa0c2f55a4)

Company: https://www.globalkeysolutions.net/companies/cardionics-inc/66b4e137-e0fb-444e-b17a-fffca655d53e

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