# Epiphany Cardiography Products – FDA Inspection, Apr 17, 2018

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

> FDA inspection 1057632 of Epiphany Cardiography Products, April 17, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- 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: 0

## Related Documents

- [FDA Inspection 929606 - 2015-06-11](https://www.keypedia.com/records/fda_inspections/epiphany-cardiography-products/8084c6ed-0f6b-490b-ab49-4d9356b9e198)
- FDA Inspection 650235 - 2010-03-05

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/joey-c-west/4ecce3be-9f8f-40eb-a7ff-0364f5864bfa)
- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

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

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