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Abdi Hakim

⚠️ High Risk

FEI: 3006372625 • Nairobi • KENYA

FEI

FEI Number

3006372625

📍

Location

Nairobi

🇰🇪

Country

KENYA
🏢

Address

P.O Box 68309, , Nairobi, , Kenya

High Risk

FDA Import Risk Assessment

51.4
LowModerateHighCritical

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

Statistics

6
Total Refusals
1
Unique Violations
5/27/2008
Latest Refusal
8/24/2007
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

116×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
5/27/2008
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
11UNSAFE COL
New Orleans District Office (NOL-DO)
1/28/2008
50NYY18HENNA
11UNSAFE COL
New Orleans District Office (NOL-DO)
1/14/2008
50NYY18HENNA
11UNSAFE COL
New Orleans District Office (NOL-DO)
1/14/2008
50NYY18HENNA
11UNSAFE COL
New Orleans District Office (NOL-DO)
8/27/2007
50NGH18HENNA
11UNSAFE COL
New Orleans District Office (NOL-DO)
8/24/2007
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
11UNSAFE COL
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Abdi Hakim's FDA import refusal history?

Abdi Hakim (FEI: 3006372625) has 6 FDA import refusal record(s) in our database, spanning from 8/24/2007 to 5/27/2008.

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. Abdi Hakim's FEI number is 3006372625.

What types of violations has Abdi Hakim received?

Abdi Hakim 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 Abdi Hakim come from?

All FDA import refusal data for Abdi Hakim 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.