Home / Import refusals / 799-9778664-7/10001/1

FDA Import Refusal 799-9778664-7/10001/1 — Angiodynamics, Inc.

Angiodynamics, Inc. — FEI 1319211

The FDA refused shipment 799-9778664-7/10001/1 from Angiodynamics, Inc. (United States) on December 4, 2025. The refused product falls under Devices — CATHETER, PERCUTANEOUS, INTRAVASCULAR, LONG TERM. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 4, 2025
Country
United States
Product Category
Devices
Product Code
80LJS CATHETER, PERCUTANEOUS, INTRAVASCULAR, LONG TERM
Charges
118,508

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

  • 799-7638247-4/11/1 (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)
  • 336-6939168-5/1/1 (Tue May 05 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources