Home / Import refusals / AEK-6187912-5/11/1

FDA Import Refusal AEK-6187912-5/11/1 — Guangdong Baihe Medical Technology Co., Ltd

Guangdong Baihe Medical Technology Co., Ltd — FEI 3006621386

The FDA refused shipment AEK-6187912-5/11/1 from Guangdong Baihe Medical Technology Co., Ltd (China) on August 21, 2019. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charges: 118,3280,508 This firm has 1 other import refusal on record.

Refusal Details

Date
August 21, 2019
Country
China
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
118,3280,508

Recent inspections

  • 1027009 (VAI Thu Aug 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 828938 (VAI Thu Mar 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 775617 (OAI Fri Mar 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 144-5247538-0/1/1 (Thu Jan 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources