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CARLOS TOBIAS RAMIREZ

⚠️ High Risk

FEI: 3031213213 • Quecholac, MEX • MEXICO

FEI

FEI Number

3031213213

📍

Location

Quecholac, MEX

🇲🇽

Country

MEXICO
🏢

Address

C9 Poniente 8 Barrio Sa, , Quecholac, MEX, Mexico

High Risk

FDA Import Risk Assessment

60.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/11/2024
Latest Refusal
6/10/2024
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
53.5×20%
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

2413×

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
6/11/2024
25JFC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
6/10/2024
25JFC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
6/10/2024
25JFC04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is CARLOS TOBIAS RAMIREZ's FDA import refusal history?

CARLOS TOBIAS RAMIREZ (FEI: 3031213213) has 3 FDA import refusal record(s) in our database, spanning from 6/10/2024 to 6/11/2024.

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. CARLOS TOBIAS RAMIREZ's FEI number is 3031213213.

What types of violations has CARLOS TOBIAS RAMIREZ received?

CARLOS TOBIAS RAMIREZ 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 CARLOS TOBIAS RAMIREZ come from?

All FDA import refusal data for CARLOS TOBIAS RAMIREZ 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.