ImportRefusal LogoImportRefusal

Melrob-Eurolabs Limited

⚠️ Moderate Risk

FEI: 3003199144 • Congleton, Cheshire • UNITED KINGDOM

FEI

FEI Number

3003199144

📍

Location

Congleton, Cheshire

🇬🇧
🏢

Address

12 John Bradshaw Court, Alexandria Way, Congleton, Cheshire, United Kingdom

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
9/26/2005
Latest Refusal
9/26/2005
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

1151×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

Refusal History

DateProductViolationsDivision
9/26/2005
61EIL04BUDESONIDE (ANTI-ASTHMATIC)
115DR QUALITY
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Melrob-Eurolabs Limited's FDA import refusal history?

Melrob-Eurolabs Limited (FEI: 3003199144) has 1 FDA import refusal record(s) in our database, spanning from 9/26/2005 to 9/26/2005.

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. Melrob-Eurolabs Limited's FEI number is 3003199144.

What types of violations has Melrob-Eurolabs Limited received?

Melrob-Eurolabs Limited 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 Melrob-Eurolabs Limited come from?

All FDA import refusal data for Melrob-Eurolabs Limited 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.