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Alcan Packaging-Baie D'urfe

⚠️ Moderate Risk

FEI: 3004329308 • Baie-D'Urfe, Quebec • CANADA

FEI

FEI Number

3004329308

📍

Location

Baie-D'Urfe, Quebec

🇨🇦

Country

CANADA
🏢

Address

19701 Clark-Graham Ave, , Baie-D'Urfe, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
4/8/2004
Latest Refusal
4/8/2004
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1791×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
4/8/2004
61JCY13PRAVASTATIN SODIUM (ANTI-CHOLESTEREMIC)
179AGR RX
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Alcan Packaging-Baie D'urfe's FDA import refusal history?

Alcan Packaging-Baie D'urfe (FEI: 3004329308) has 1 FDA import refusal record(s) in our database, spanning from 4/8/2004 to 4/8/2004.

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. Alcan Packaging-Baie D'urfe's FEI number is 3004329308.

What types of violations has Alcan Packaging-Baie D'urfe received?

Alcan Packaging-Baie D'urfe 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 Alcan Packaging-Baie D'urfe come from?

All FDA import refusal data for Alcan Packaging-Baie D'urfe 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.