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FDA Inspection 620119 — AngioDynamics, Inc.

AngioDynamics, Inc. — FEI 3017892510

The FDA completed an inspection of AngioDynamics, Inc. on September 30, 2009 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
September 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Glens Falls, NY (United States)

Facility

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