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
Bioresearch Monitoring
Location
Warsaw, IN (United States)

Additional Details

Postmarket Audit Inspections