ImportRefusal LogoImportRefusal

BENESSI LABS

⚠️ High Risk

FEI: 3024848027 • Cortes • HONDURAS

FEI

FEI Number

3024848027

📍

Location

Cortes

🇭🇳

Country

HONDURAS
🏢

Address

1 Kilmetro Norte De San, , Cortes, , Honduras

High Risk

FDA Import Risk Assessment

51.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
10/27/2025
Latest Refusal
10/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
95.7×20%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

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
10/27/2025
60ZDY02ALBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is BENESSI LABS's FDA import refusal history?

BENESSI LABS (FEI: 3024848027) has 1 FDA import refusal record(s) in our database, spanning from 10/27/2025 to 10/27/2025.

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. BENESSI LABS's FEI number is 3024848027.

What types of violations has BENESSI LABS received?

BENESSI LABS has been cited for 2 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 BENESSI LABS come from?

All FDA import refusal data for BENESSI LABS 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.