FDA Inspection 1263001 — Ardeshir R. Rastinehad, D.O.

Ardeshir R. Rastinehad, D.O. — FEI 3030989339

The FDA completed an inspection of Ardeshir R. Rastinehad, D.O. on Feb 28, 2025 in New York, NY. 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). Product area: Devices.