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Carlos Carrillo Redonsel

⚠️ Moderate Risk

FEI: 3001049006 • Mex • MEXICO

FEI

FEI Number

3001049006

📍

Location

Mex

🇲🇽

Country

MEXICO
🏢

Address

No. 208 Colonia Centro, , Guaymas Son, Mex, , Mexico

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
11/15/2002
Latest Refusal
11/15/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

2492×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
11/15/2002
16JDD05SHRIMP & PRAWNS
249FILTHY
473LABELING
Southwest Import District Office (SWI-DO)
11/15/2002
16MGD14SNAILS, AQUATIC, OTHER AQUATIC SPECIES
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Carlos Carrillo Redonsel's FDA import refusal history?

Carlos Carrillo Redonsel (FEI: 3001049006) has 2 FDA import refusal record(s) in our database, spanning from 11/15/2002 to 11/15/2002.

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 Carrillo Redonsel's FEI number is 3001049006.

What types of violations has Carlos Carrillo Redonsel received?

Carlos Carrillo Redonsel has been cited for 2 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 Carrillo Redonsel come from?

All FDA import refusal data for Carlos Carrillo Redonsel 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.