FDA Inspection 940561 — Robert J. Kreitman, MD

Robert J. Kreitman, MD — FEI 3003786134

The FDA completed an inspection of Robert J. Kreitman, MD on Aug 28, 2015 in Bethesda, 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: Drugs.