FDA Inspection 575030 — Aranda Juan, MD

Aranda Juan, MD — FEI 3007209619

The FDA completed an inspection of Aranda Juan, MD on Mar 26, 2009 in Gainesville, 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.