FDA Inspection 754158 — Tornier, Inc

Tornier, Inc — FEI 3000718467

The FDA completed an inspection of Tornier, Inc on Nov 3, 2011 in Bloomington, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 3, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)