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FDA Inspection 1223219 — Biomet, Inc.

Biomet, Inc. — FEI 1825034

The FDA completed an inspection of Biomet, Inc. on November 9, 2023 in Warsaw, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 9, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)

Facility

Other inspections at this facility

  • 1116404 (NAI Thu Jan 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1050097 (NAI Tue Apr 24 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998381 (OAI Tue Nov 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885336 (NAI Mon Jun 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 654579 (NAI Fri Mar 26 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources