FDA Inspection 735887 — AngioDynamics, Inc.

AngioDynamics, Inc. — FEI 3017892510

The FDA completed an inspection of AngioDynamics, Inc. on July 12, 2011 in Glens Falls, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 12, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Glens Falls, NY (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation