FDA Inspection 1011987 — Kerendi Faraz, MD

Kerendi Faraz, MD — FEI 3013367811

The FDA completed an inspection of Kerendi Faraz, MD on May 25, 2017 in Austin, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.