FDA Inspection 844677 — Zimmer, Inc.

Zimmer, Inc. — FEI 1000220733

The FDA completed an inspection of Zimmer, Inc. on August 19, 2013 in Warsaw, IN. 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 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)