# FDA Inspection 1011987 - Kerendi Faraz, MD - May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/kerendi-faraz-md/0717e7b9-79f0-4cba-bec3-bf397e8f8a2a
Source feed: FDA_Inspections

> FDA Inspection 1011987 for Kerendi Faraz, MD on May 25, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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