FDA Inspection 753667 — Cheryl M. Burgess, MD

Cheryl M. Burgess, MD — FEI 3009226944

The FDA completed an inspection of Cheryl M. Burgess, MD on Nov 10, 2011 in Washington, DC. 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.