Home / Import refusals / AEK-7888202-1/11/1

FDA Import Refusal AEK-7888202-1/11/1 — Haupt Pharma Latina Srl

Haupt Pharma Latina Srl — FEI 3007687501

The FDA refused shipment AEK-7888202-1/11/1 from Haupt Pharma Latina Srl (Italy) on October 20, 2020. The refused product falls under Drugs and Biologics — SERTRALINE HYDROCHLORIDE (ANTI-DEPRESSANT). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
October 20, 2020
Country
Italy
Product Category
Drugs and Biologics
Product Code
61NCA78 SERTRALINE HYDROCHLORIDE (ANTI-DEPRESSANT)
Charges
75

Recent inspections

  • 1237210 (OAI Wed Feb 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1206882 (VAI Fri Jul 29 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1059418 (VAI Thu Jun 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1004993 (VAI Fri Dec 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 908678 (VAI Tue Nov 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-5660756-5/21/1 (Fri Sep 20 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-5505089-0/41/1 (Thu Jul 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-4467796-3/11/1 (Wed Apr 28 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-8772002-2/11/1 (Fri Feb 26 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-4001717-8/51/1 (Thu Jan 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources