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FDA Inspection 1085752 — Invacare Corporation

Invacare Corporation — FEI 1000220413

The FDA completed an inspection of Invacare Corporation on March 8, 2019 in North Ridgeville, 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
March 8, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Ridgeville, OH (United States)

Facility

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  • 1118888 (NAI Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1015890 (NAI Wed Jun 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources