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FDA Import Refusal UPS-3589723-2/1/1 — Sterex Electrolysis Int Ltd

Sterex Electrolysis Int Ltd — FEI 1000439607

The FDA refused shipment UPS-3589723-2/1/1 from Sterex Electrolysis Int Ltd (United Kingdom) on February 4, 2014. The refused product falls under Devices — EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE. Cited charge: 2780 This firm has 4 other import refusals on record.

Refusal Details

Date
February 4, 2014
Country
United Kingdom
Product Category
Devices
Product Code
79KCW EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE
Charges
2780

Recent inspections

  • 904085 (NAI Thu Nov 06 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821451 (OAI Thu Feb 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 112-0229977-5/1/1 (Thu Dec 06 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)
  • 112-6234370-2/1/1 (Thu May 10 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)
  • 112-2381323-1/2/2 (Mon Sep 11 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)
  • 112-2381323-1/2/1 (Mon Sep 11 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)

FDA data resources