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A Sukded

⚠️ Moderate Risk

FEI: 3003313124 • Annandale • GUYANA

FEI

FEI Number

3003313124

📍

Location

Annandale

🇬🇾

Country

GUYANA
🏢

Address

137 Courbane Mark, , Annandale, , Guyana

Moderate Risk

FDA Import Risk Assessment

36.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
3/12/2004
Latest Refusal
8/29/2002
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
13.0×10%
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

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

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.

Refusal History

DateProductViolationsDivision
3/12/2004
16AFC45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2960FALSECAT
New York District Office (NYK-DO)
8/29/2002
16AGC35SHARK
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is A Sukded's FDA import refusal history?

A Sukded (FEI: 3003313124) has 2 FDA import refusal record(s) in our database, spanning from 8/29/2002 to 3/12/2004.

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. A Sukded's FEI number is 3003313124.

What types of violations has A Sukded received?

A Sukded 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 A Sukded come from?

All FDA import refusal data for A Sukded 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.