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FDA Import Refusal 336-7475237-8/51/1 — GRI Medical & Electronic Technology Co., Ltd.

GRI Medical & Electronic Technology Co., Ltd. — FEI 3004911384

The FDA refused shipment 336-7475237-8/51/1 from GRI Medical & Electronic Technology Co., Ltd. (China) on May 17, 2022. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 17, 2022
Country
China
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,341

Recent inspections

  • 989002 (NAI Thu Sep 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 896201 (NAI Thu Aug 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 813361 (OAI Thu Dec 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

FDA data resources