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ANA MARIA NAVARRO ROBLES

⚠️ High Risk

FEI: 3017170211 • Quecholac • MEXICO

FEI

FEI Number

3017170211

📍

Location

Quecholac

🇲🇽

Country

MEXICO
🏢

Address

Palmarito, Calle Jose Maria Morelo; Puebla, El Carmen, Quecholac, , Mexico

High Risk

FDA Import Risk Assessment

62.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
1
Unique Violations
7/7/2025
Latest Refusal
6/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
74.9×20%
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
7/7/2025
25JHC07RADISH (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
6/27/2025
20NGC05PRICKLE PEAR (CORE FRUIT)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is ANA MARIA NAVARRO ROBLES's FDA import refusal history?

ANA MARIA NAVARRO ROBLES (FEI: 3017170211) has 2 FDA import refusal record(s) in our database, spanning from 6/27/2025 to 7/7/2025.

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. ANA MARIA NAVARRO ROBLES's FEI number is 3017170211.

What types of violations has ANA MARIA NAVARRO ROBLES received?

ANA MARIA NAVARRO ROBLES 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 ANA MARIA NAVARRO ROBLES come from?

All FDA import refusal data for ANA MARIA NAVARRO ROBLES 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.