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A Kopman

⚠️ Moderate Risk

FEI: 3004180623 • North York, ON • CANADA

FEI

FEI Number

3004180623

📍

Location

North York, ON

🇨🇦

Country

CANADA
🏢

Address

33 Purdon Dr, , North York, ON, Canada

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
11/20/2003
Latest Refusal
11/20/2003
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
11/20/2003
66VBB99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)
11/20/2003
66VBB99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is A Kopman's FDA import refusal history?

A Kopman (FEI: 3004180623) has 2 FDA import refusal record(s) in our database, spanning from 11/20/2003 to 11/20/2003.

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. A Kopman's FEI number is 3004180623.

What types of violations has A Kopman received?

A Kopman 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 A Kopman come from?

All FDA import refusal data for A Kopman 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.