Home / Import refusals / AEK-5249546-0/11/1

FDA Import Refusal AEK-5249546-0/11/1 — Bayer Weimar GmbH und Co. KG

Bayer Weimar GmbH und Co. KG — FEI 3002808091

The FDA refused shipment AEK-5249546-0/11/1 from Bayer Weimar GmbH und Co. KG (Germany) on May 15, 2024. The refused product falls under Drugs and Biologics — NORETHINDRONE (PROGESTIN). Cited charges: 118,3280,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 15, 2024
Country
Germany
Product Category
Drugs and Biologics
Product Code
65JCY24 NORETHINDRONE (PROGESTIN)
Charges
118,3280,75

Recent inspections

  • 1274501 (VAI Thu Nov 24 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1101920 (VAI Fri Sep 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 948310 (NAI Thu Nov 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 805216 (NAI Fri Oct 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 636510 (VAI Fri Dec 04 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-9054196-1/10002/1 (Wed May 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9170474-0/10002/1 (Tue Jan 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-6778468-0/41/1 (Mon Nov 04 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-2553843-2/21/1 (Fri Aug 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-5414997-4/11/1 (Sun Aug 04 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources