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FDA Inspection 598332 — Howmedica Osteonics Corp.

Howmedica Osteonics Corp. — FEI 3003070421

The FDA completed an inspection of Howmedica Osteonics Corp. on July 20, 2009 in Mahwah, NJ. 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
July 20, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Mahwah, NJ (United States)

Facility

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