FDA Inspection 773793 — Castellvi Antonio, MD

Castellvi Antonio, MD — FEI 3007183631

The FDA completed an inspection of Castellvi Antonio, MD on Mar 21, 2012 in Tampa, FL. 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.