FDA Inspection 559842 — Invacare Corporation

Invacare Corporation — FEI 3002889431

The FDA completed an inspection of Invacare Corporation on Dec 19, 2008 in Elyria, OH. 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
Dec 19, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Elyria, OH (United States)

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