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Grupo Imbrium S.A. De C.V.

⚠️ Moderate Risk

FEI: 3003650770 • San Luis Potosi, SLP • MEXICO

FEI

FEI Number

3003650770

📍

Location

San Luis Potosi, SLP

🇲🇽

Country

MEXICO
🏢

Address

Sierra Negra No. 125 Lomas 3ro Secc., , San Luis Potosi, SLP, Mexico

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/13/2004
Latest Refusal
7/15/2003
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
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

2493×

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
2/13/2004
24HFH08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
11/7/2003
24HFH08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
7/15/2003
24HFH08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Grupo Imbrium S.A. De C.V.'s FDA import refusal history?

Grupo Imbrium S.A. De C.V. (FEI: 3003650770) has 3 FDA import refusal record(s) in our database, spanning from 7/15/2003 to 2/13/2004.

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. Grupo Imbrium S.A. De C.V.'s FEI number is 3003650770.

What types of violations has Grupo Imbrium S.A. De C.V. received?

Grupo Imbrium S.A. De C.V. 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 Grupo Imbrium S.A. De C.V. come from?

All FDA import refusal data for Grupo Imbrium 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.