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Akhavan

⚠️ Moderate Risk

FEI: 3003849944 • Saint-Laurent, QC • CANADA

FEI

FEI Number

3003849944

📍

Location

Saint-Laurent, QC

🇨🇦

Country

CANADA
🏢

Address

4355 Poirier St, , Saint-Laurent, QC, Canada

Moderate Risk

FDA Import Risk Assessment

28.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
8/15/2005
Latest Refusal
4/21/2003
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
8.6×10%
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

2971×

AFLATOXIN

The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.

3281×

USUAL NAME

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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
8/15/2005
23BFT11PISTACHIO, SHELLED
297AFLATOXIN
New York District Office (NYK-DO)
4/21/2003
24UGH21PARSLEY, DRIED OR PASTE
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)

Frequently Asked Questions

What is Akhavan's FDA import refusal history?

Akhavan (FEI: 3003849944) has 2 FDA import refusal record(s) in our database, spanning from 4/21/2003 to 8/15/2005.

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. Akhavan's FEI number is 3003849944.

What types of violations has Akhavan received?

Akhavan 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 Akhavan come from?

All FDA import refusal data for Akhavan 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.