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Atre Abidjan

⚠️ Moderate Risk

FEI: 3027566179 • Abidjan, Ci-Ab • IVORY COAST

FEI

FEI Number

3027566179

📍

Location

Abidjan, Ci-Ab

🇨🇮
🏢

Address

Cocody Riviera Palmeraie, , Abidjan, Ci-Ab, Ivory Coast

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
9/5/2023
Latest Refusal
9/5/2023
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
53.0×20%
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

3281×

USUAL NAME

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
9/5/2023
25QGH04MUSHROOM, SHIITAKE, PIECES AND STEMS, SLICED
328USUAL NAME
9SALMONELLA
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Atre Abidjan's FDA import refusal history?

Atre Abidjan (FEI: 3027566179) has 1 FDA import refusal record(s) in our database, spanning from 9/5/2023 to 9/5/2023.

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. Atre Abidjan's FEI number is 3027566179.

What types of violations has Atre Abidjan received?

Atre Abidjan has been cited for 2 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 Atre Abidjan come from?

All FDA import refusal data for Atre Abidjan 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.