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Duroseau Fernabde

⚠️ Moderate Risk

FEI: 3005384868 • Port-Au-Prince, ouest • HAITI

FEI

FEI Number

3005384868

📍

Location

Port-Au-Prince, ouest

🇭🇹

Country

HAITI
🏢

Address

Drand Rue 237, , Port-Au-Prince, ouest, Haiti

Moderate Risk

FDA Import Risk Assessment

27.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
12/27/2005
Latest Refusal
12/27/2005
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

4734×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
12/27/2005
36BHT08SUGAR SYRUP, BEET AND CANE (LIQUID SUCROSE, SIMPLE SYRUP)
473LABELING
Florida District Office (FLA-DO)
12/27/2005
53JK01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
473LABELING
Florida District Office (FLA-DO)
12/27/2005
02HAT02CORN STARCH
473LABELING
Florida District Office (FLA-DO)
12/27/2005
02DAT01RICE, BROWN, PROCESSED (PACKAGED)
473LABELING
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Duroseau Fernabde's FDA import refusal history?

Duroseau Fernabde (FEI: 3005384868) has 4 FDA import refusal record(s) in our database, spanning from 12/27/2005 to 12/27/2005.

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. Duroseau Fernabde's FEI number is 3005384868.

What types of violations has Duroseau Fernabde received?

Duroseau Fernabde 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 Duroseau Fernabde come from?

All FDA import refusal data for Duroseau Fernabde 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.