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FDA Import Refusal AEK-3630448-0/11/1 — Karl Storz SE & Co. KG

Karl Storz SE & Co. KG — FEI 3002808268

The FDA refused shipment AEK-3630448-0/11/1 from Karl Storz SE & Co. KG (Germany) on August 29, 2017. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
August 29, 2017
Country
Germany
Product Category
Devices
Product Code
79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Charges
341

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Other import refusals

  • 799-3908548-7/11/1 (Thu Oct 24 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-8406978-9/21/2 (Fri Sep 04 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-4512432-6/11/1 (Tue Mar 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-8403234-7/11/1 (Fri Jan 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 336-9581332-3/1/1 (Tue Oct 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

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