FDA Inspection 737505 — Invacare Corporation

Invacare Corporation — FEI 1031452

The FDA completed an inspection of Invacare Corporation on Jul 27, 2011 in Sanford, FL. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sanford, FL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
317221 CFR 820.198(c)Investigation of device failures
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation
77121 CFR 803.52(e)(1)Contact Office Name and Address

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