FDA Inspection 700347 — Edward Snyder, MD

Edward Snyder, MD — FEI 3007358802

The FDA completed an inspection of Edward Snyder, MD on Nov 22, 2010 in New Haven, CT. 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: Biologics.