Home / Import refusals / AEK-0468492-3/10002/1

FDA Import Refusal AEK-0468492-3/10002/1 — Mt.Derm Gmbh

Mt.Derm Gmbh — FEI 3006634874

The FDA refused shipment AEK-0468492-3/10002/1 from Mt.Derm Gmbh (Germany) on May 21, 2026. The refused product falls under Devices — POWERED MICRONEEDLE DEVICE. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 21, 2026
Country
Germany
Product Category
Devices
Product Code
79QAI POWERED MICRONEEDLE DEVICE
Charges
118,508

Recent inspections

  • 1196535 (VAI Thu Jan 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • SCS-4427643-8/11/1 (Wed Jun 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-9193829-3/11/1 (Sun Aug 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • F47-0074654-4/41/1 (Fri Jun 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-2837407-3/11/1 (Mon Apr 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0765924-2/1/1 (Wed Oct 21 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources