FDA Inspection 1019513 — Invacare Corporation

Invacare Corporation — FEI 1525712

The FDA completed an inspection of Invacare Corporation on Jun 16, 2017 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
Jun 16, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Elyria, OH (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.