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Arlen Nibbs

⚠️ Moderate Risk

FEI: 3003630632 • Roadtown • BRITISH VIRGIN ISLANDS

FEI

FEI Number

3003630632

📍

Location

Roadtown

🇻🇬
🏢

Address

Akara Bldg Cay 1, , Roadtown, , British Virgin Islands

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/13/2002
Latest Refusal
6/13/2002
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

3312×

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
6/13/2002
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)
6/13/2002
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Arlen Nibbs's FDA import refusal history?

Arlen Nibbs (FEI: 3003630632) has 2 FDA import refusal record(s) in our database, spanning from 6/13/2002 to 6/13/2002.

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. Arlen Nibbs's FEI number is 3003630632.

What types of violations has Arlen Nibbs received?

Arlen Nibbs 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 Arlen Nibbs come from?

All FDA import refusal data for Arlen Nibbs 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.