Home / Import refusals / 300-1955154-9/10001/1

FDA Import Refusal 300-1955154-9/10001/1 — Midmark Corporation

Midmark Corporation — FEI 3000210017

The FDA refused shipment 300-1955154-9/10001/1 from Midmark Corporation (United States) on December 16, 2025. The refused product falls under Devices — SYSTEM, X-RAY, EXTRAORAL SOURCE, DIGITAL. Cited charges: 118,3280,341,508 This firm has 2 other import refusals on record.

Refusal Details

Date
December 16, 2025
Country
United States
Product Category
Devices
Product Code
90MUH SYSTEM, X-RAY, EXTRAORAL SOURCE, DIGITAL
Charges
118,3280,341,508

Recent inspections

  • 1234396 (NAI Thu Mar 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1026007 (NAI Tue Aug 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 770816 (NAI Tue Mar 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 648559 (VAI Wed Feb 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • BON-1004700-9/7/2 (Mon May 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • F81-0187812-9/1/1 (Thu Mar 28 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources