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ALEJANDRA SANTIAGO PALMA

⚠️ Moderate Risk

FEI: 2000040381 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

2000040381

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Peatonal Retorno 3 Epsilon 9-414, Col. Romero De Terreros, Coyoacan, Ciudad De Mexico, Ciudad de Mexico, 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
2/5/2009
Latest Refusal
2/5/2009
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

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.

Refusal History

DateProductViolationsDivision
2/5/2009
24FFH08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
249FILTHY
New York District Office (NYK-DO)
2/5/2009
24FFH08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is ALEJANDRA SANTIAGO PALMA's FDA import refusal history?

ALEJANDRA SANTIAGO PALMA (FEI: 2000040381) has 2 FDA import refusal record(s) in our database, spanning from 2/5/2009 to 2/5/2009.

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. ALEJANDRA SANTIAGO PALMA's FEI number is 2000040381.

What types of violations has ALEJANDRA SANTIAGO PALMA received?

ALEJANDRA SANTIAGO PALMA 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 ALEJANDRA SANTIAGO PALMA come from?

All FDA import refusal data for ALEJANDRA SANTIAGO PALMA 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.