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AW Products

⚠️ Moderate Risk

FEI: 3005081352 • Boisbriand, Quebec • CANADA

FEI

FEI Number

3005081352

📍

Location

Boisbriand, Quebec

🇨🇦

Country

CANADA
🏢

Address

PO Box 60056, 875 Grande-Allee, Boisbriand, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
4/18/2005
Latest Refusal
4/18/2005
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

2603×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
4/18/2005
13YHT99ICE CREAM AND RELATED PRODUCTS, N.E.C.
260FALSE
New York District Office (NYK-DO)
4/18/2005
13FHT99ICES, FRUIT FLAVORED, N.E.C.
260FALSE
New York District Office (NYK-DO)
4/18/2005
13FHT99ICES, FRUIT FLAVORED, N.E.C.
260FALSE
New York District Office (NYK-DO)

Frequently Asked Questions

What is AW Products's FDA import refusal history?

AW Products (FEI: 3005081352) has 3 FDA import refusal record(s) in our database, spanning from 4/18/2005 to 4/18/2005.

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. AW Products's FEI number is 3005081352.

What types of violations has AW Products received?

AW Products 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 AW Products come from?

All FDA import refusal data for AW Products 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.