FDA Inspection 787548 — Steven Kantrow, MD

Steven Kantrow, MD — FEI 3009423442

The FDA completed an inspection of Steven Kantrow, MD on Jun 20, 2012 in New Orleans, LA. 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.