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FDA Import Refusal 112-5663339-0/1/1 — Angiodynamics, Inc.

Angiodynamics, Inc. — FEI 1319211

The FDA refused shipment 112-5663339-0/1/1 from Angiodynamics, Inc. (United States) on January 20, 2009. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 118,476 This firm has 5 or more other import refusals on record.

Refusal Details

Date
January 20, 2009
Country
United States
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
118,476

Recent inspections

  • 1258185 (VAI Fri Jan 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979520 (VAI Thu Apr 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 866566 (OAI Tue Feb 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 801850 (OAI Mon Sep 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756504 (OAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 799-9778664-7/10001/1 (Thu Dec 04 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-7638247-4/11/1 (Fri May 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Radiological Health)
  • 336-6938742-8/1/1 (Tue May 05 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 336-6938742-8/1/2 (Tue May 05 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 336-6938742-8/1/3 (Tue May 05 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources