FDA Inspection 872141 — Tornier, Inc

Tornier, Inc — FEI 3000718467

The FDA completed an inspection of Tornier, Inc on Mar 26, 2014 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
Mar 26, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bloomington, MN (United States)

Additional Details

Sponsor, Contract Research Organization