FDA Inspection 650242 — Sheinkop, Mitchell, B, Md

Sheinkop, Mitchell, B, Md — FEI 3008089312

The FDA completed an inspection of Sheinkop, Mitchell, B, Md on Feb 10, 2010 in Chicago, IL. 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: Devices.