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FDA Inspection 587353 — DePuy Orthopaedics, Inc.

DePuy Orthopaedics, Inc. — FEI 1818910

The FDA completed an inspection of DePuy Orthopaedics, Inc. on June 1, 2009 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
June 1, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)

Facility

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Recent compliance actions

FDA data resources