FDA Inspection 681078 — Warsaw Orthopedic, Inc.

Warsaw Orthopedic, Inc. — FEI 1824199

The FDA completed an inspection of Warsaw Orthopedic, Inc. on Aug 20, 2010 in Warsaw, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 20, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Warsaw, IN (United States)

Additional Details

Postmarket Audit Inspections