FDA Inspection 799272 — Schilling, Kathy, MD

Schilling, Kathy, MD — FEI 3009674529

The FDA completed an inspection of Schilling, Kathy, MD on Sep 18, 2012 in Boca Raton, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.