FDA Inspection 781540 — ConMed Corporation

ConMed Corporation — FEI 3001451571

The FDA completed an inspection of ConMed Corporation on April 26, 2012 in Utica, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Utica, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
369621 CFR 820.100(b)Documentation