# Epiphany Cardiography Products – FDA Inspection, Jun 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/epiphany-cardiography-products/8084c6ed-0f6b-490b-ab49-4d9356b9e198
Source feed: FDA_Inspections

> FDA inspection 929606 of Epiphany Cardiography Products, June 11, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 929606
- Company Name: Epiphany Cardiography Products
- Inspection Date: 2015-06-11
- 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 1057632 - 2018-04-17](https://www.keypedia.com/records/fda_inspections/epiphany-cardiography-products/c5fa4cf5-1083-4597-a4f6-c560b151a7de)
- FDA Inspection 650235 - 2010-03-05

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