FDA Inspection 780731 — Steven H. Dayan, MD

Steven H. Dayan, MD — FEI 3008692411

The FDA completed an inspection of Steven H. Dayan, MD on Sep 21, 2012 in Chicago, IL. 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.