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Abayaa Enterprise Limited

⚠️ Moderate Risk

FEI: 3004482351 • Accra • GHANA

FEI

FEI Number

3004482351

📍

Location

Accra

🇬🇭

Country

GHANA
🏢

Address

P.o. Box 2784, , Dansoman, Accra, , Ghana

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/16/2004
Latest Refusal
8/16/2004
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

29601×

FALSECAT

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because it purports to be or is represented as catfish but is not a fish classified within the family Ictaluridae.

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
8/16/2004
16IFN10CATFISH, FRESHWATER, HOT SMOKED (E.G. CHANNEL, BLUE, WHITE, YAQUI, BULLHEAD, FLATHEAD CATFISH)
2960FALSECAT
308MFR INSAN
New York District Office (NYK-DO)

Frequently Asked Questions

What is Abayaa Enterprise Limited's FDA import refusal history?

Abayaa Enterprise Limited (FEI: 3004482351) has 1 FDA import refusal record(s) in our database, spanning from 8/16/2004 to 8/16/2004.

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. Abayaa Enterprise Limited's FEI number is 3004482351.

What types of violations has Abayaa Enterprise Limited received?

Abayaa Enterprise Limited 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 Abayaa Enterprise Limited come from?

All FDA import refusal data for Abayaa Enterprise Limited 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.