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Berlex Canada Inc

⚠️ Moderate Risk

FEI: 3004196896 • Pointe-Claire, QUEBEC • CANADA

FEI

FEI Number

3004196896

📍

Location

Pointe-Claire, QUEBEC

🇨🇦

Country

CANADA
🏢

Address

334 Ave Avro, , Pointe-Claire, QUEBEC, Canada

Moderate Risk

FDA Import Risk Assessment

38.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
1/28/2009
Latest Refusal
11/1/2006
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
8.9×10%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
1/28/2009
61BCA02CYPROTERONE ACETATE (ANTI-ANDROGEN)
75UNAPPROVED
New York District Office (NYK-DO)
11/1/2006
85HDTDEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER
237NO PMA
84RX DEVICE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Berlex Canada Inc's FDA import refusal history?

Berlex Canada Inc (FEI: 3004196896) has 2 FDA import refusal record(s) in our database, spanning from 11/1/2006 to 1/28/2009.

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. Berlex Canada Inc's FEI number is 3004196896.

What types of violations has Berlex Canada Inc received?

Berlex Canada Inc has been cited for 3 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 Berlex Canada Inc come from?

All FDA import refusal data for Berlex Canada Inc 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.