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HECHO EN MEXICO POR LABORATORIOS

⚠️ High Risk

FEI: 3021716694 • Cuajimalpa De Morelos • MEXICO

FEI

FEI Number

3021716694

📍

Location

Cuajimalpa De Morelos

🇲🇽

Country

MEXICO
🏢

Address

Adolfo Lopez Mateos No, , Cuajimalpa De Morelos, , Mexico

High Risk

FDA Import Risk Assessment

58.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
1/6/2026
Latest Refusal
1/6/2026
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
91.0×20%
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

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
1/6/2026
54AFL16VITAMIN E (TOCOPHEROL)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HECHO EN MEXICO POR LABORATORIOS's FDA import refusal history?

HECHO EN MEXICO POR LABORATORIOS (FEI: 3021716694) has 1 FDA import refusal record(s) in our database, spanning from 1/6/2026 to 1/6/2026.

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. HECHO EN MEXICO POR LABORATORIOS's FEI number is 3021716694.

What types of violations has HECHO EN MEXICO POR LABORATORIOS received?

HECHO EN MEXICO POR LABORATORIOS 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 HECHO EN MEXICO POR LABORATORIOS come from?

All FDA import refusal data for HECHO EN MEXICO POR LABORATORIOS 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.