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FDA Import Refusal UPS-4651684-6/51/1 — Medtronic Neuromodulation

Medtronic Neuromodulation — FEI 2182207

The FDA refused shipment UPS-4651684-6/51/1 from Medtronic Neuromodulation (United States) on August 29, 2017. The refused product falls under Devices — STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF. Cited charge: 3280 This firm has 3 other import refusals on record.

Refusal Details

Date
August 29, 2017
Country
United States
Product Category
Devices
Product Code
84LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
Charges
3280

Recent inspections

  • 1206222 (VAI Fri May 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1187313 (VAI Thu Nov 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1153966 (NAI Thu Sep 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1108789 (VAI Thu Oct 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102180 (NAI Tue Aug 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • UPS-4651684-6/91/1 (Tue Aug 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-4651684-6/41/1 (Tue Aug 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-1296829-2/1/1 (Tue Feb 18 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources