# MyCardio – FDA Inspection, Jun 26, 2017

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

> FDA inspection 1015573 of MyCardio, June 26, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1015573
- Company Name: MyCardio
- Inspection Date: 2017-06-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1106057 - 2018-07-18](https://www.keypedia.com/records/fda_inspections/mycardio/539cdcdb-dd3d-4f46-a05b-5ef3ea882e06)
- FDA Inspection 805529 - 2012-10-22

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

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