Home / Inspections / 828384

FDA Inspection 828384 — AngioDynamics, Inc.

AngioDynamics, Inc. — FEI 3017892510

The FDA completed an inspection of AngioDynamics, Inc. on November 28, 2012 in Glens Falls, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 28, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Glens Falls, NY (United States)

Facility

Other inspections at this facility

  • 1145201 (VAI Fri Jun 25 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 967909 (VAI Fri Apr 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941614 (VAI Thu Aug 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))

FDA data resources