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FDA Import Refusal 799-1294538-1/11/1D — Angiomed GmbH & Co. Medizintechnik KG

Angiomed GmbH & Co. Medizintechnik KG — FEI 3002806368

The FDA refused shipment 799-1294538-1/11/1D from Angiomed GmbH & Co. Medizintechnik KG (Germany) on June 6, 2019. The refused product falls under Devices — STENT, SUPERFICIAL FEMORAL ARTERY. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
June 6, 2019
Country
Germany
Product Category
Devices
Product Code
74NIP STENT, SUPERFICIAL FEMORAL ARTERY
Charges
118,3280

Recent inspections

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  • 953098 (NAI Thu Aug 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 812973 (NAI Thu Dec 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 676642 (NAI Thu Mar 25 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • UPS-3441674-3/1/1 (Mon Sep 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-3362653-2/1/1 (Tue Sep 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-3298276-1/1/1 (Wed Sep 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-3278139-5/1/1 (Wed Sep 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-3340482-3/1/1 (Wed Sep 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources