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STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES

⚠️ High Risk

FEI: 3019731941 • MOROCCO

FEI

FEI Number

3019731941

📍

Location

—

🇲🇦

Country

MOROCCO
🏢

Address

AVENUE HASSAN II NR 11ER ETAGE SOUK SEBT., , Fquih Ben Salah (M),, , Morocco

High Risk

FDA Import Risk Assessment

56.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
1/31/2024
Latest Refusal
1/31/2024
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
60.6×20%
Frequency
10.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
1/31/2024
20GFC11CLEMENTINE (CITRUS)
241PESTICIDE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES's FDA import refusal history?

STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES (FEI: 3019731941) has 1 FDA import refusal record(s) in our database, spanning from 1/31/2024 to 1/31/2024.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES's FEI number is 3019731941.

What types of violations has STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES received?

STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES come from?

All FDA import refusal data for STE ASMAA DEMBALLAGE ET DEXPORTATION DES AGRUMES is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.