FDA Inspection 572415 — Zimmer, Inc.

Zimmer, Inc. — FEI 1000220733

The FDA completed an inspection of Zimmer, Inc. on March 19, 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
March 19, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)