FDA Inspection 900329 — Invacare Corporation

Invacare Corporation — FEI 1031452

The FDA completed an inspection of Invacare Corporation on October 20, 2014 in Sanford, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 20, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Sanford, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation
53721 CFR 820.70(a)Production processes