Home / Import refusals / AEK-9254299-0/10001/1

FDA Import Refusal AEK-9254299-0/10001/1 — Merck & Co. Inc

Merck & Co. Inc — FEI 2211017

The FDA refused shipment AEK-9254299-0/10001/1 from Merck & Co. Inc (United States) on January 28, 2026. The refused product falls under Drugs and Biologics — BETAMETHASONE (GLUCOCORTICOID). Cited charges: 118,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
January 28, 2026
Country
United States
Product Category
Drugs and Biologics
Product Code
64LCY03 BETAMETHASONE (GLUCOCORTICOID)
Charges
118,75

Recent inspections

  • 1305632 (NAI Fri Mar 13 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1283890 (NAI Thu Dec 18 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1262774 (NAI Fri May 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1264192 (NAI Thu Mar 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1158317 (NAI Thu Nov 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • AEK-7515529-9/10002/1 (Wed Aug 13 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7462726-4/30001/1 (Tue Aug 05 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-6705454-8/91/1 (Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-5766294-0/11/1 (Sat Nov 09 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-7987432-0/11/1 (Tue Jun 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources