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Rodolfo Perez

⚠️ Moderate Risk

FEI: 3008902848 • San Luis De La Paz, Guanajuato • MEXICO

FEI

FEI Number

3008902848

📍

Location

San Luis De La Paz, Guanajuato

🇲🇽

Country

MEXICO
🏢

Address

Calle Allende 313, Col. San Luis De La Paz Centro, San Luis De La Paz, San Luis De La Paz, Guanajuato, Mexico

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
4/3/2012
Latest Refusal
12/13/2011
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2412×

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
4/3/2012
24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)
12/13/2011
24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Rodolfo Perez's FDA import refusal history?

Rodolfo Perez (FEI: 3008902848) has 2 FDA import refusal record(s) in our database, spanning from 12/13/2011 to 4/3/2012.

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. Rodolfo Perez's FEI number is 3008902848.

What types of violations has Rodolfo Perez received?

Rodolfo Perez 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 Rodolfo Perez come from?

All FDA import refusal data for Rodolfo Perez 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.