FDA Inspection 803305 — Ronald E. Delanois, MD

Ronald E. Delanois, MD — FEI 3009789386

The FDA completed an inspection of Ronald E. Delanois, MD on Oct 17, 2012 in Baltimore, MD. 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). 1 citation was issued during this inspection. Product area: Devices.