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FDA Import Refusal 8K4-0072145-0/51/1 — MICROVENTION INC.

MICROVENTION INC. — FEI 3013556777

The FDA refused shipment 8K4-0072145-0/51/1 from MICROVENTION INC. (United States) on April 8, 2025. The refused product falls under Devices — WIRE, GUIDE, CATHETER. Cited charge: 3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
April 8, 2025
Country
United States
Product Category
Devices
Product Code
74DQX WIRE, GUIDE, CATHETER
Charges
3280

Recent inspections

  • 1205080 (VAI Thu May 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1155400 (NAI Tue Jun 22 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1074141 (NAI Thu Nov 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 943775 (VAI Fri Sep 25 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 757144 (NAI Tue Dec 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-6103491-6/11/1 (Tue Apr 15 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-6103491-6/11/2 (Tue Apr 15 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-6103491-6/11/3 (Tue Apr 15 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-6103491-6/11/4 (Tue Apr 15 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-5952412-6/21/1 (Mon Mar 24 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources