FDA Inspection 677464 — Invacare Corporation

Invacare Corporation — FEI 1031452

The FDA completed an inspection of Invacare Corporation on August 18, 2010 in Sanford, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 18, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Sanford, FL (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures
319221 CFR 820.30(g)Design validation - user needs and intended uses
367121 CFR 820.25(a)Personnel
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
369621 CFR 820.100(b)Documentation
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements