# FDA Inspection 650235 - Epiphany Cardiography Products - March 05, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/813b06ec-09ea-4bfa-88d2-ca7914656095
Source feed: FDA_Inspections

> FDA Inspection 650235 for Epiphany Cardiography Products on March 05, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 650235
- Company Name: Epiphany Cardiography Products
- Inspection Date: 2010-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 650235 - 2010-03-05](https://www.globalkeysolutions.net/records/fda_inspections/epiphany-cardiography-products/85c836dc-6a79-4eb6-86c4-178538abefdf)

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