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PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V.

⚠️ Moderate Risk

FEI: 2000003986 • Villa De Alvarez, Colima • MEXICO

FEI

FEI Number

2000003986

📍

Location

Villa De Alvarez, Colima

🇲🇽

Country

MEXICO
🏢

Address

Prolongacion Cristobal Colon 1036, , Villa De Alvarez, Colima, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
4/17/2009
Latest Refusal
4/17/2009
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2491×

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
4/17/2009
21SHB14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT)
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V.'s FDA import refusal history?

PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V. (FEI: 2000003986) has 1 FDA import refusal record(s) in our database, spanning from 4/17/2009 to 4/17/2009.

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. PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V.'s FEI number is 2000003986.

What types of violations has PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V. received?

PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V. 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 PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V. come from?

All FDA import refusal data for PRODUCTOS INDUSTRIALIZADOS TECOMAN S.A. DE C.V. 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.