Home / Import refusals / 799-6175365-2/11/1

FDA Import Refusal 799-6175365-2/11/1 — BioFire Diagnostics, LLC

BioFire Diagnostics, LLC — FEI 3002773840

The FDA refused shipment 799-6175365-2/11/1 from BioFire Diagnostics, LLC (United States) on March 30, 2020. The refused product falls under Devices — INSTRUMENTATION FOR CLINICAL MULIPLEX TEST SYSTEMS. Cited charges: 118,3280,341 This firm has 2 other import refusals on record.

Refusal Details

Date
March 30, 2020
Country
United States
Product Category
Devices
Product Code
75NSU INSTRUMENTATION FOR CLINICAL MULIPLEX TEST SYSTEMS
Charges
118,3280,341

Recent inspections

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  • 678758 (NAI Thu Aug 05 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-6361426-6/11/1 (Thu Apr 23 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-5260540-8/11/1 (Wed Mar 04 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources