# FDA Inspection 1057632 - Epiphany Cardiography Products - April 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/c5fa4cf5-1083-4597-a4f6-c560b151a7de
Source feed: FDA_Inspections

> FDA Inspection 1057632 for Epiphany Cardiography Products on April 17, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057632
- Company Name: Epiphany Cardiography Products
- Inspection Date: 2018-04-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 929606 - 2015-06-11](https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/8084c6ed-0f6b-490b-ab49-4d9356b9e198)
- [FDA Inspection 650235 - 2010-03-05](https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/85c836dc-6a79-4eb6-86c4-178538abefdf)
- [FDA Inspection 650235 - 2010-03-05](https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/813b06ec-09ea-4bfa-88d2-ca7914656095)

Company: https://www.globalkeysolutions.net/companies/epiphany-cardiography-products/a2749e58-2955-439e-a519-0ad5dd2e86fc

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