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NORIDEL S.A.

⚠️ High Risk

FEI: 3010938177 • Salto, Salto • URUGUAY

FEI

FEI Number

3010938177

📍

Location

Salto, Salto

🇺🇾

Country

URUGUAY
🏢

Address

Avenida Jose Garibaldi 2350, , Salto, Salto, Uruguay

High Risk

FDA Import Risk Assessment

59.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/11/2023
Latest Refusal
6/13/2023
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
49.9×20%
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

2413×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
7/11/2023
20GFC11CLEMENTINE (CITRUS)
241PESTICIDE
Division of Northeast Imports (DNEI)
6/29/2023
20GFC11CLEMENTINE (CITRUS)
241PESTICIDE
Division of Northeast Imports (DNEI)
6/13/2023
20GFC11CLEMENTINE (CITRUS)
241PESTICIDE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

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

NORIDEL S.A. (FEI: 3010938177) has 3 FDA import refusal record(s) in our database, spanning from 6/13/2023 to 7/11/2023.

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. NORIDEL S.A.'s FEI number is 3010938177.

What types of violations has NORIDEL S.A. received?

NORIDEL S.A. 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 NORIDEL S.A. come from?

All FDA import refusal data for NORIDEL S.A. 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.