FDA Inspection 654579 — Biomet, Inc.

Biomet, Inc. — FEI 1825034

The FDA completed an inspection of Biomet, Inc. on March 26, 2010 in Warsaw, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 26, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Warsaw, IN (United States)

Additional Details

Sponsor, Contract Research Organization