Home / Import refusals / FR1-0018322-2/61/1

FDA Import Refusal FR1-0018322-2/61/1 — AQUISEL S.L.U.

AQUISEL S.L.U. — FEI 3010352064

The FDA refused shipment FR1-0018322-2/61/1 from AQUISEL S.L.U. (Spain) on June 14, 2022. The refused product falls under Devices — TEST, ERYTHROCYTE SEDIMENTATION RATE. Cited charge: 118 This firm has 4 other import refusals on record.

Refusal Details

Date
June 14, 2022
Country
Spain
Product Category
Devices
Product Code
81JPH TEST, ERYTHROCYTE SEDIMENTATION RATE
Charges
118

Recent inspections

  • 1090088 (VAI Wed May 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • FR1-0018508-6/71/1 (Wed Aug 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018248-9/101/1 (Tue Jan 11 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018257-0/121/1 (Tue Sep 14 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0015523-8/1/1 (Thu Apr 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources