FDA Inspection 559842 — Invacare Corporation

Invacare Corporation — FEI 3002889431

The FDA completed an inspection of Invacare Corporation on December 19, 2008 in Elyria, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 19, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Elyria, OH (United States)