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FDA Inspection 941614 — AngioDynamics, Inc.

AngioDynamics, Inc. — FEI 3017892510

The FDA completed an inspection of AngioDynamics, Inc. on August 13, 2015 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
August 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Glens Falls, NY (United States)

Facility

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  • 887029 (VAI Tue Jul 15 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 866897 (VAI Sun Mar 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 828384 (NAI Wed Nov 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources