Home / Import refusals / AEK-7480778-2/21/1

FDA Import Refusal AEK-7480778-2/21/1 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808208

The FDA refused shipment AEK-7480778-2/21/1 from Sanofi Winthrop Industrie (France) on June 19, 2020. The refused product falls under Drugs and Biologics — IRBESARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
June 19, 2020
Country
France
Product Category
Drugs and Biologics
Product Code
62OCE37 IRBESARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

Recent inspections

  • 1267532 (VAI Wed Nov 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094501 (VAI Fri Apr 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 861974 (VAI Fri Dec 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 753776 (NAI Fri Nov 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 560525 (VAI Fri Jan 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-0516922-1/10002/1 (Wed Jun 10 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0272725-2/10002/2 (Thu Apr 16 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9378844-4/10002/1 (Thu Feb 19 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9124494-5/20002/1 (Wed Dec 17 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7507384-9/10002/1 (Thu Sep 04 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

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