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Dudley Larocque

⚠️ Moderate Risk

FEI: 3007506885 • St Maartenst Maarten • SINT MAARTEN

FEI

FEI Number

3007506885

📍

Location

St Maartenst Maarten

🇸🇽
🏢

Address

Tunis Dr. # 6l. P. Q., , St Maartenst Maarten, , Sint Maarten

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
5/4/2009
Latest Refusal
5/4/2009
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

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
5/4/2009
66VCC99MISCELLANEOUS PATENT MEDICINES, ETC.
336INCONSPICU
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Dudley Larocque's FDA import refusal history?

Dudley Larocque (FEI: 3007506885) has 1 FDA import refusal record(s) in our database, spanning from 5/4/2009 to 5/4/2009.

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. Dudley Larocque's FEI number is 3007506885.

What types of violations has Dudley Larocque received?

Dudley Larocque 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 Dudley Larocque come from?

All FDA import refusal data for Dudley Larocque 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.