FDA Inspection 707297 — ConMed Corporation

ConMed Corporation — FEI 3001451571

The FDA completed an inspection of ConMed Corporation on January 26, 2011 in Utica, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 26, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Utica, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
319221 CFR 820.30(g)Design validation - user needs and intended uses
369621 CFR 820.100(b)Documentation