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AGMEL S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3011280733 • Monterrey, Nuevo Leon • MEXICO

FEI

FEI Number

3011280733

📍

Location

Monterrey, Nuevo Leon

🇲🇽

Country

MEXICO
🏢

Address

Calle Helsinki 5213, Col. Las Torres, Monterrey, Monterrey, Nuevo Leon, Mexico

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/5/2012
Latest Refusal
9/5/2012
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

2491×

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.

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
9/5/2012
36ACB99SUGAR PRODUCTS, N.E.C.
249FILTHY
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is AGMEL S.A. DE C.V.'s FDA import refusal history?

AGMEL S.A. DE C.V. (FEI: 3011280733) has 1 FDA import refusal record(s) in our database, spanning from 9/5/2012 to 9/5/2012.

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. AGMEL S.A. DE C.V.'s FEI number is 3011280733.

What types of violations has AGMEL S.A. DE C.V. received?

AGMEL S.A. DE C.V. 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 AGMEL S.A. DE C.V. come from?

All FDA import refusal data for AGMEL S.A. DE C.V. 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.