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PATIENCE AKHIDNOR

⚠️ Moderate Risk

FEI: 3007079273 • Lagos, Lagos • NIGERIA

FEI

FEI Number

3007079273

📍

Location

Lagos, Lagos

🇳🇬

Country

NIGERIA
🏢

Address

12 Akinsanya St., , Lagos, Lagos, Nigeria

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/9/2012
Latest Refusal
2/8/2012
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4823×

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
6/9/2012
34BFT99CHOCOLATE AND COCOA, N.E.C.
482NUTRIT LBL
Division of Northeast Imports (DNEI)
2/8/2012
29BCT99CARBONATED SOFT DRINK, N.E.C.
482NUTRIT LBL
Division of Northeast Imports (DNEI)
2/8/2012
28YGT99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C.
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is PATIENCE AKHIDNOR's FDA import refusal history?

PATIENCE AKHIDNOR (FEI: 3007079273) has 3 FDA import refusal record(s) in our database, spanning from 2/8/2012 to 6/9/2012.

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. PATIENCE AKHIDNOR's FEI number is 3007079273.

What types of violations has PATIENCE AKHIDNOR received?

PATIENCE AKHIDNOR 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 PATIENCE AKHIDNOR come from?

All FDA import refusal data for PATIENCE AKHIDNOR 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.