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P. F. L. M. SA DE CV

⚠️ High Risk

FEI: 3005115332 • Los Mochis, Sinaloa • MEXICO

FEI

FEI Number

3005115332

📍

Location

Los Mochis, Sinaloa

🇲🇽

Country

MEXICO
🏢

Address

Avenida Revolucion Pte 440, Fracc. Jiquilpan, Ahome, Los Mochis, Sinaloa, Mexico

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
12/16/2005
Latest Refusal
12/16/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2494×

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
12/16/2005
16JEO01CRAB
249FILTHY
Southwest Import District Office (SWI-DO)
12/16/2005
16JEO01CRAB
249FILTHY
Southwest Import District Office (SWI-DO)
12/16/2005
16JEO01CRAB
249FILTHY
Southwest Import District Office (SWI-DO)
12/16/2005
16JEO01CRAB
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is P. F. L. M. SA DE CV's FDA import refusal history?

P. F. L. M. SA DE CV (FEI: 3005115332) has 4 FDA import refusal record(s) in our database, spanning from 12/16/2005 to 12/16/2005.

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. P. F. L. M. SA DE CV's FEI number is 3005115332.

What types of violations has P. F. L. M. SA DE CV received?

P. F. L. M. SA DE CV 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 P. F. L. M. SA DE CV come from?

All FDA import refusal data for P. F. L. M. SA DE CV 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.