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FDA Inspection 845339 — Zimmer Manufacturing B.V.

Zimmer Manufacturing B.V. — FEI 1000132037

The FDA completed an inspection of Zimmer Manufacturing B.V. on August 16, 2013 in Mercedita, PR. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 16, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mercedita, PR (United States)

Facility

Other inspections at this facility

  • 1133679 (NAI Thu Oct 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1019065 (VAI Thu Jul 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950318 (VAI Tue Nov 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 884721 (OAI Wed Jun 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 822907 (OAI Fri May 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources