FDA Inspection 590433 — Lumen Biomedical, Inc.

Lumen Biomedical, Inc. — FEI 3005522028

The FDA completed an inspection of Lumen Biomedical, Inc. on Jun 18, 2009 in Maple Grove, MN. 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.