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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.