FDA Inspection 1001740 — Edward M. Geltman, MD

Edward M. Geltman, MD — FEI 3012068244

The FDA completed an inspection of Edward M. Geltman, MD on Jan 30, 2017 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.