FDA Inspection 760707 — iScreen Vision, Inc.

iScreen Vision, Inc. — FEI 3003004358

The FDA completed an inspection of iScreen Vision, Inc. on Dec 21, 2011 in Cordova, TN. 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.