FDA Inspection 866897 — AngioDynamics, Inc.

AngioDynamics, Inc. — FEI 3017892510

The FDA completed an inspection of AngioDynamics, Inc. on March 30, 2014 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Glens Falls, NY (United States)