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Shiiraar Abukar

Low Risk

FEI: 3003786680 • Mogadishu • SOMALIA

FEI

FEI Number

3003786680

📍

Location

Mogadishu

🇸🇴

Country

SOMALIA
🏢

Address

Bakara Market, , Mogadishu, , Somalia

Low Risk

FDA Import Risk Assessment

18.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
5/6/2003
Latest Refusal
5/6/2003
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
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

3201×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
5/6/2003
26CGT09SESAME OIL, REFINED, SINGLE INGREDIENT
320LACKS FIRM
482NUTRIT LBL
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Shiiraar Abukar's FDA import refusal history?

Shiiraar Abukar (FEI: 3003786680) has 1 FDA import refusal record(s) in our database, spanning from 5/6/2003 to 5/6/2003.

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. Shiiraar Abukar's FEI number is 3003786680.

What types of violations has Shiiraar Abukar received?

Shiiraar Abukar 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 Shiiraar Abukar come from?

All FDA import refusal data for Shiiraar Abukar 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.