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Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl

⚠️ Moderate Risk

FEI: 3008718522 • Ciudad Del Maiz, San Luis Potosi • MEXICO

FEI

FEI Number

3008718522

📍

Location

Ciudad Del Maiz, San Luis Potosi

🇲🇽

Country

MEXICO
🏢

Address

Gomez Palacios S/N Ej Palomas, Col. CIUDAD DEL MAIZ CENTRO, Ciudad Del Maiz, San Luis Potosi, Mexico

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
12/29/2022
Latest Refusal
2/7/2011
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
17.7×30%
Recency
24.0×20%
Frequency
1.7×10%
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

20402×

SULFITELBL

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
12/29/2022
52BYY06CORN HUSKS (FOOD RELATED)
2040SULFITELBL
Division of Southwest Imports (DSWI)
2/7/2011
52BYY06CORN HUSKS (FOOD RELATED)
2040SULFITELBL
218LIST INGRE
320LACKS FIRM
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl's FDA import refusal history?

Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl (FEI: 3008718522) has 2 FDA import refusal record(s) in our database, spanning from 2/7/2011 to 12/29/2022.

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 Agropecuario La Parcela Del Mmaiz S De Pr De Rl's FEI number is 3008718522.

What types of violations has Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl received?

Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl has been cited for 3 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 Agropecuario La Parcela Del Mmaiz S De Pr De Rl come from?

All FDA import refusal data for Grupo Agropecuario La Parcela Del Mmaiz S De Pr De Rl 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.