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Lordi S. A. U

✅ Low Risk

FEI: 3004277038 • Los Yebenes, Toledo • SPAIN

FEI

FEI Number

3004277038

📍

Location

Los Yebenes, Toledo

🇪🇸

Country

SPAIN
🏢

Address

Parcela 1, Poligono Industrial La Canada, Los Yebenes, Toledo, Spain

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/30/2014
Latest Refusal
9/30/2014
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

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
9/30/2014
12CGP15CHEESE, GOAT, N.E.C.
3320TRANSFAT
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Lordi S. A. U's FDA import refusal history?

Lordi S. A. U (FEI: 3004277038) has 1 FDA import refusal record(s) in our database, spanning from 9/30/2014 to 9/30/2014.

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. Lordi S. A. U's FEI number is 3004277038.

What types of violations has Lordi S. A. U received?

Lordi S. A. U 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 Lordi S. A. U come from?

All FDA import refusal data for Lordi S. A. U 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.