# FDA Inspection 1015573 - MyCardio - June 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/mycardio/4c756b32-21b9-482a-b3d5-059ffc24b38b
Source feed: FDA_Inspections

> FDA Inspection 1015573 for MyCardio on June 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015573
- Company Name: MyCardio
- Inspection Date: 2017-06-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1015573 - 2017-06-26](https://www.keypedia.com/records/fda_inspections/mycardio/09d9972b-5f5e-41c3-936a-77d22069a7b5)
- [FDA Inspection 805529 - 2012-10-22](https://www.keypedia.com/records/fda_inspections/mycardio/f2684bd1-ebdf-4aa3-9b2c-d724776d8fb8)
- [FDA Inspection 805529 - 2012-10-22](https://www.keypedia.com/records/fda_inspections/mycardio/a8b1922b-f9af-4bb0-860d-383ce825e6dd)

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