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Lauro Garcia Aguilera SPR de RL de CV

⚠️ Moderate Risk

FEI: 2000003991 • La Ribera, Jalisco • MEXICO

FEI

FEI Number

2000003991

📍

Location

La Ribera, Jalisco

🇲🇽

Country

MEXICO
🏢

Address

Calle Lazaro Cardenas 11, Ayotlan, La Ribera, Jalisco, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/7/2019
Latest Refusal
11/7/2019
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

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
11/7/2019
24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Lauro Garcia Aguilera SPR de RL de CV's FDA import refusal history?

Lauro Garcia Aguilera SPR de RL de CV (FEI: 2000003991) has 1 FDA import refusal record(s) in our database, spanning from 11/7/2019 to 11/7/2019.

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. Lauro Garcia Aguilera SPR de RL de CV's FEI number is 2000003991.

What types of violations has Lauro Garcia Aguilera SPR de RL de CV received?

Lauro Garcia Aguilera SPR de RL de CV 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 Lauro Garcia Aguilera SPR de RL de CV come from?

All FDA import refusal data for Lauro Garcia Aguilera SPR de RL de CV 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.