# CardioFocus, Inc. – FDA Inspection, Jun 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/cardiofocus-inc/e81f4e09-e208-4f12-a3a6-2e0940c526b7
Source feed: FDA_Inspections

> FDA inspection 1016613 of CardioFocus, Inc., June 30, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016613
- Company Name: CardioFocus, Inc.
- Inspection Date: 2017-06-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1177544 - 2022-08-11
- FDA Inspection 928695 - 2015-05-07
- FDA Inspection 808977 - 2012-11-28
- FDA Inspection 746966 - 2011-09-23

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nabil-nakhoul/d676e9c9-566c-4e59-84e8-1dc474e4e48d)

Company: https://www.keypedia.com/companies/cardiofocus-inc/49750a9c-aa39-4080-bfaa-4edc4912b956

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