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FDA Import Refusal 799-7266025-9/11/1 — Carefusion 2200 Inc

Carefusion 2200 Inc — FEI 3008002452

The FDA refused shipment 799-7266025-9/11/1 from Carefusion 2200 Inc (United States) on August 23, 2018. The refused product falls under Devices — CATHETER, PERCUTANEOUS. Cited charges: 118,341

Refusal Details

Date
August 23, 2018
Country
United States
Product Category
Devices
Product Code
74DQY CATHETER, PERCUTANEOUS
Charges
118,341

Recent inspections

  • 1181731 (VAI Wed Oct 19 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1078836 (NAI Thu Nov 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 926924 (VAI Thu May 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855080 (OAI Tue Nov 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 743357 (VAI Wed Sep 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

FDA data resources