ImportRefusal LogoImportRefusal

ALHIKMA EST

⚠️ Moderate Risk

FEI: 3026973215 • Kuwait City • KUWAIT

FEI

FEI Number

3026973215

📍

Location

Kuwait City

🇰🇼

Country

KUWAIT
🏢

Address

Aljeean Center Kheetan, , Kuwait City, , Kuwait

Moderate Risk

FDA Import Risk Assessment

26.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
5/11/2023
Latest Refusal
5/11/2023
Earliest Refusal

Score Breakdown

Violation Severity
33.3×40%
Refusal Volume
11.2×30%
Recency
46.0×20%
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

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
5/11/2023
36CYY99HONEY, N.E.C.
321LACKS N/C
324NO ENGLISH
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ALHIKMA EST's FDA import refusal history?

ALHIKMA EST (FEI: 3026973215) has 1 FDA import refusal record(s) in our database, spanning from 5/11/2023 to 5/11/2023.

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. ALHIKMA EST's FEI number is 3026973215.

What types of violations has ALHIKMA EST received?

ALHIKMA EST has been cited for 3 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 ALHIKMA EST come from?

All FDA import refusal data for ALHIKMA EST 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.