# FDA Inspection 805529 - MyCardio - October 22, 2012

Source: https://www.keypedia.com/records/fda_inspections/mycardio/f2684bd1-ebdf-4aa3-9b2c-d724776d8fb8
Source feed: FDA_Inspections

> FDA Inspection 805529 for MyCardio on October 22, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805529
- Company Name: MyCardio
- Inspection Date: 2012-10-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/mycardio/4dd43f03-4c2e-4c5c-8881-e309ce01b976

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