Home / Import refusals / DY2-0049282-4/11/1

FDA Import Refusal DY2-0049282-4/11/1 — Henan Kangdi Medical Devices Co. Ltd

Henan Kangdi Medical Devices Co. Ltd — FEI 3009271465

The FDA refused shipment DY2-0049282-4/11/1 from Henan Kangdi Medical Devices Co. Ltd (China) on June 5, 2017. The refused product falls under Cosmetics — CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
June 5, 2017
Country
China
Product Category
Cosmetics
Product Code
53LD01 CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
Charges
75

Recent inspections

  • 1084134 (OAI Thu Mar 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 995883 (VAI Wed Dec 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • M34-2224793-2/11/1 (Fri Dec 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 051-0227077-3/11/2 (Mon Oct 28 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 002-7133166-2/12/1 (Mon Aug 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)
  • 002-7133166-2/12/2 (Mon Aug 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Cosmetics)
  • DY2-0049306-1/11/1 (Wed Jul 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources