Home / Import refusals / 110-0640179-4/5/1

FDA Import Refusal 110-0640179-4/5/1 — Clarity Diagnostics, LLC

Clarity Diagnostics, LLC — FEI 3004043187

The FDA refused shipment 110-0640179-4/5/1 from Clarity Diagnostics, LLC (United States) on November 7, 2007. The refused product falls under Devices — REAGENT, OCCULT BLOOD. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 7, 2007
Country
United States
Product Category
Devices
Product Code
81KHE REAGENT, OCCULT BLOOD
Charges
341

Recent inspections

  • 1169763 (NAI Wed Apr 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1088913 (VAI Wed May 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833184 (VAI Thu May 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 110-0640179-4/1/1A (Wed Nov 07 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 110-0640179-4/1/1B (Wed Nov 07 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 110-0640179-4/1/1C (Wed Nov 07 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 110-0640179-4/1/1D (Wed Nov 07 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 110-0640179-4/4/1 (Wed Nov 07 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources