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AL NADA EXPO

⚠️ Moderate Risk

FEI: 3013423442 • KUWAIT CITY • KUWAIT

FEI

FEI Number

3013423442

📍

Location

KUWAIT CITY

🇰🇼

Country

KUWAIT
🏢

Address

AL ZAHARA BLOCK 4, ST 4, , KUWAIT CITY, , Kuwait

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
5/10/2017
Latest Refusal
5/10/2017
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
5/10/2017
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
508NO 510(K)
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AL NADA EXPO's FDA import refusal history?

AL NADA EXPO (FEI: 3013423442) has 1 FDA import refusal record(s) in our database, spanning from 5/10/2017 to 5/10/2017.

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. AL NADA EXPO's FEI number is 3013423442.

What types of violations has AL NADA EXPO received?

AL NADA EXPO 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 AL NADA EXPO come from?

All FDA import refusal data for AL NADA EXPO 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.