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HECHO EN MEXICO PRO PRODUCTOS

⚠️ Moderate Risk

FEI: 3020245182 • Juarez • MEXICO

FEI

FEI Number

3020245182

📍

Location

Juarez

🇲🇽

Country

MEXICO
🏢

Address

Nicola San Juan 1045 Co, , Juarez, , Mexico

Moderate Risk

FDA Import Risk Assessment

40.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/12/2021
Latest Refusal
10/12/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
1.0×20%
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
10/12/2021
60LCA05ASPIRIN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HECHO EN MEXICO PRO PRODUCTOS's FDA import refusal history?

HECHO EN MEXICO PRO PRODUCTOS (FEI: 3020245182) has 1 FDA import refusal record(s) in our database, spanning from 10/12/2021 to 10/12/2021.

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 PRO PRODUCTOS's FEI number is 3020245182.

What types of violations has HECHO EN MEXICO PRO PRODUCTOS received?

HECHO EN MEXICO PRO PRODUCTOS 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 PRO PRODUCTOS come from?

All FDA import refusal data for HECHO EN MEXICO PRO PRODUCTOS 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.