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Jean Raphael Lamarque

⚠️ Moderate Risk

FEI: 3003942570 • Port-Au-Prince, ouest • HAITI

FEI

FEI Number

3003942570

📍

Location

Port-Au-Prince, ouest

🇭🇹

Country

HAITI
🏢

Address

Rue 3, , Port-Au-Prince, ouest, Haiti

Moderate Risk

FDA Import Risk Assessment

39.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
2/5/2004
Latest Refusal
12/8/2003
Earliest Refusal

Score Breakdown

Violation Severity
68.6×40%
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

4732×

LABELING

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

752×

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).

20801×

COUMARIN

The article appears to bear or contain Coumarin, a poisonous or deleterious substance, which may render it injurious to health.

2491×

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.

3241×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
2/5/2004
25RAH07MUSHROOM, CHANTERELLE, BROKEN OR KIBBLED
249FILTHY
473LABELING
Florida District Office (FLA-DO)
12/8/2003
28MHT04VANILLA (VANILLIN) IMITATION FLAVOR
2080COUMARIN
324NO ENGLISH
473LABELING
Florida District Office (FLA-DO)
12/8/2003
65SCL01RUBBING ALCOHOL (RUBEFACIENT)
75UNAPPROVED
Florida District Office (FLA-DO)
12/8/2003
65SCL01RUBBING ALCOHOL (RUBEFACIENT)
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Jean Raphael Lamarque's FDA import refusal history?

Jean Raphael Lamarque (FEI: 3003942570) has 4 FDA import refusal record(s) in our database, spanning from 12/8/2003 to 2/5/2004.

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. Jean Raphael Lamarque's FEI number is 3003942570.

What types of violations has Jean Raphael Lamarque received?

Jean Raphael Lamarque has been cited for 5 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 Jean Raphael Lamarque come from?

All FDA import refusal data for Jean Raphael Lamarque 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.