FDA Inspection 816055 — 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 February 19, 2013 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.