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FDA Import Refusal SCS-2018381-2/11/1 — CELLRETURN CO., LTD

CELLRETURN CO., LTD — FEI 3016883165

The FDA refused shipment SCS-2018381-2/11/1 from CELLRETURN CO., LTD (South Korea) on September 28, 2020. The refused product falls under Devices — OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 28, 2020
Country
South Korea
Product Category
Devices
Product Code
79OLP OVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
Charges
118,3280,508

Other import refusals

  • 799-8364711-5/11/1 (Thu Apr 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-6577927-6/11/1 (Fri Aug 13 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-6226617-8/11/1 (Tue Jul 13 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-3372617-7/11/1 (Thu Dec 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-2798491-5/11/1 (Tue Nov 10 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources