FDA Inspection 1040982 — Hormozd Bozorgchami, MD

Hormozd Bozorgchami, MD — FEI 3013833459

The FDA completed an inspection of Hormozd Bozorgchami, MD on Feb 7, 2018 in Portland, OR. 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.