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FDA Inspection 1085712 — Invacare Corporation

Invacare Corporation — FEI 1525712

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

Facility

Other inspections at this facility

  • 1203095 (NAI Thu Mar 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1147199 (OAI Thu Jun 24 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1118985 (VAI Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1019513 (NAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 951244 (OAI Wed Dec 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources