FDA Inspection 910826 — Tornier Inc.

Tornier Inc. — FEI 3004983210

The FDA completed an inspection of Tornier Inc. on Jan 22, 2015 in Columbia City, IN. 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
Jan 22, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia City, IN (United States)