# Kerendi Faraz, MD – FDA Inspection, May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/kerendi-faraz-md/61007ae2-26fc-4442-9c66-e2f5a5339729
Source feed: FDA_Inspections

> FDA inspection 1011987 of Kerendi Faraz, MD, May 25, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1011987
- Company Name: Kerendi Faraz, MD
- Inspection Date: 2017-05-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/camille-d-brown/419869d2-1810-40ea-8e8a-687de7013f6a)

Company: https://www.keypedia.com/companies/kerendi-faraz-md/b65c0be7-6d34-4141-aa97-ec7fb4977b17

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