Home / Import refusals / 799-1200056-9/11/1

FDA Import Refusal 799-1200056-9/11/1 — Medtronic Inc

Medtronic Inc — FEI 3001504994

The FDA refused shipment 799-1200056-9/11/1 from Medtronic Inc (United States) on October 12, 2022. The refused product falls under Devices — DRILL, BATTERY POWERED, SUBUNGUAL HEMATOMA. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
October 12, 2022
Country
United States
Product Category
Devices
Product Code
79NWF DRILL, BATTERY POWERED, SUBUNGUAL HEMATOMA
Charges
118,3280

Other import refusals

  • AEK-9259307-6/10001/1 (Wed Jan 28 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-7007961-5/11/1 (Mon Dec 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-1292228-4/11/1 (Fri Jun 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-4445661-2/31/1 (Fri Dec 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-4513404-4/11/1 (Mon Dec 18 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources