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Uraeus Group

⚠️ Moderate Risk

FEI: 3003823710 • Scotland • UNITED KINGDOM

FEI

FEI Number

3003823710

📍

Location

Scotland

🇬🇧
🏢

Address

Po Box 786, , Scotland, , United Kingdom

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
3/18/2003
Latest Refusal
3/18/2003
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

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

Refusal History

DateProductViolationsDivision
3/18/2003
66BBL05CAFFEINE (STIMULANT)
223FALSE
331DR QUALITC
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Uraeus Group's FDA import refusal history?

Uraeus Group (FEI: 3003823710) has 1 FDA import refusal record(s) in our database, spanning from 3/18/2003 to 3/18/2003.

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. Uraeus Group's FEI number is 3003823710.

What types of violations has Uraeus Group received?

Uraeus Group 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 Uraeus Group come from?

All FDA import refusal data for Uraeus Group 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.