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La Lupa

⚠️ High Risk

FEI: 3003414381 • Rutigliano, BA • ITALY

FEI

FEI Number

3003414381

📍

Location

Rutigliano, BA

🇮🇹

Country

ITALY
🏢

Address

Strada Statale 634, , Rutigliano, BA, Italy

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
12/13/2001
Latest Refusal
10/16/2001
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2414×

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
12/13/2001
20AGB09GRAPES (BERRY)
241PESTICIDE
New York District Office (NYK-DO)
10/16/2001
20AGB09GRAPES (BERRY)
241PESTICIDE
New York District Office (NYK-DO)
10/16/2001
20AGB09GRAPES (BERRY)
241PESTICIDE
New York District Office (NYK-DO)
10/16/2001
20AGB09GRAPES (BERRY)
241PESTICIDE
New York District Office (NYK-DO)

Frequently Asked Questions

What is La Lupa's FDA import refusal history?

La Lupa (FEI: 3003414381) has 4 FDA import refusal record(s) in our database, spanning from 10/16/2001 to 12/13/2001.

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. La Lupa's FEI number is 3003414381.

What types of violations has La Lupa received?

La Lupa 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 La Lupa come from?

All FDA import refusal data for La Lupa 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.