FAUSTIN JOSEPH
⚠️ Moderate Risk
FEI: 3022454740 • Port Qu Prince • HAITI
FEI Number
3022454740
Location
Port Qu Prince
Country
HAITIAddress
Cite Militaire, , Port Qu Prince, , Haiti
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
Frequently Asked Questions
What is FAUSTIN JOSEPH's FDA import refusal history?
FAUSTIN JOSEPH (FEI: 3022454740) has 1 FDA import refusal record(s) in our database, spanning from 1/5/2024 to 1/5/2024.
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. FAUSTIN JOSEPH's FEI number is 3022454740.
What types of violations has FAUSTIN JOSEPH received?
FAUSTIN JOSEPH 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 FAUSTIN JOSEPH come from?
All FDA import refusal data for FAUSTIN JOSEPH 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.