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FDA Import Refusal 799-1006137-3/21/1 — FUJIFILM Healthcare Americas Corporation

FUJIFILM Healthcare Americas Corporation — FEI 2431293

The FDA refused shipment 799-1006137-3/21/1 from FUJIFILM Healthcare Americas Corporation (United States) on October 12, 2022. The refused product falls under Devices — TAPE, TELEVISION & VIDEO, CLOSED-CIRCUIT, USED DURING ENDOSCOPIC PROCEDURE. Cited charges: 118,3280,341 This firm has 4 other import refusals on record.

Refusal Details

Date
October 12, 2022
Country
United States
Product Category
Devices
Product Code
78FET TAPE, TELEVISION & VIDEO, CLOSED-CIRCUIT, USED DURING ENDOSCOPIC PROCEDURE
Charges
118,3280,341

Recent inspections

  • 1094948 (VAI Tue Jul 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 922868 (OAI Thu Apr 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 864022 (VAI Thu Jan 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 706457 (VAI Mon Dec 13 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 799-8849490-1/11/1 (Mon May 09 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-8243218-7/11/1 (Fri Sep 04 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-1037326-9/1/1 (Wed Apr 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-0646946-7/1/1 (Fri Feb 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources