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AGA PRODUCTORA SA DE CV

⚠️ High Risk

FEI: 3017717837 • Colonia Juarez, Oaxaca • MEXICO

FEI

FEI Number

3017717837

📍

Location

Colonia Juarez, Oaxaca

🇲🇽

Country

MEXICO
🏢

Address

Oaxaca De Juarez, San Mateo Del Mar, Colonia Juarez, Oaxaca, Mexico

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
1/15/2021
Latest Refusal
1/15/2021
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

2494×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
1/15/2021
24HGT08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Division of Southeast Imports (DSEI)
1/15/2021
24HGT08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Division of Southeast Imports (DSEI)
1/15/2021
24HGT08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Division of Southeast Imports (DSEI)
1/15/2021
24HGT08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AGA PRODUCTORA SA DE CV's FDA import refusal history?

AGA PRODUCTORA SA DE CV (FEI: 3017717837) has 4 FDA import refusal record(s) in our database, spanning from 1/15/2021 to 1/15/2021.

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. AGA PRODUCTORA SA DE CV's FEI number is 3017717837.

What types of violations has AGA PRODUCTORA SA DE CV received?

AGA PRODUCTORA SA 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 AGA PRODUCTORA SA DE CV come from?

All FDA import refusal data for AGA PRODUCTORA SA 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.