FDA Inspection 740649 — Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.)

Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.) — FEI 2183620

The FDA completed an inspection of Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.) on August 23, 2011 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.