Home / Import refusals / AEK-1676092-6/11/1

FDA Import Refusal AEK-1676092-6/11/1 — CURALLUX LLC

CURALLUX LLC — FEI 3010123655

The FDA refused shipment AEK-1676092-6/11/1 from CURALLUX LLC (United States) on September 2, 2022. The refused product falls under Devices — LAMP, INFRARED, THERAPEUTIC HEATING. Cited charges: 118,3280,47

Refusal Details

Date
September 2, 2022
Country
United States
Product Category
Devices
Product Code
89ILY LAMP, INFRARED, THERAPEUTIC HEATING
Charges
118,3280,47

Recent inspections

  • 1086640 (NAI Wed Apr 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 971370 (VAI Tue May 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 900767 (OAI Fri Nov 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 829251 (OAI Thu May 16 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

FDA data resources