FDA Inspection 1129759 — ConMed Corporation

ConMed Corporation — FEI 3001451571

The FDA completed an inspection of ConMed Corporation on September 22, 2020 in Utica, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 22, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Utica, NY (United States)