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Arthur Epicerie Fine

⚠️ Moderate Risk

FEI: 3008732378 • Montr�al, QC • CANADA

FEI

FEI Number

3008732378

📍

Location

Montr�al, QC

🇨🇦

Country

CANADA
🏢

Address

1832 Rue Sherbrooke E, , Montr�al, QC, Canada

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

8
Total Refusals
5
Unique Violations
6/17/2011
Latest Refusal
6/17/2011
Earliest Refusal

Score Breakdown

Violation Severity
60.9×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
80.0×10%
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

4827×

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.

626×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

836×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

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.

Refusal History

DateProductViolationsDivision
6/17/2011
25JCE01CARROT (ROOT & TUBER VEGETABLE)
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
24TGT10CAULIFLOWER (LEAF & STEM VEGETABLE)
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
25JGT01CARROT (ROOT & TUBER VEGETABLE)
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
24EGT14STRINGBEANS, BEAN AND PEA SPROUTS
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
24KGT20CUCUMBERS, WITH SAUCE
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
21CGT99MIXED FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C.
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
6/17/2011
37KCE99PASTES, N.E.C.
473LABELING
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/17/2011
20LCE06ORANGE, TOPPING OR SYRUP,
328USUAL NAME
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Arthur Epicerie Fine's FDA import refusal history?

Arthur Epicerie Fine (FEI: 3008732378) has 8 FDA import refusal record(s) in our database, spanning from 6/17/2011 to 6/17/2011.

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. Arthur Epicerie Fine's FEI number is 3008732378.

What types of violations has Arthur Epicerie Fine received?

Arthur Epicerie Fine has been cited for 5 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 Arthur Epicerie Fine come from?

All FDA import refusal data for Arthur Epicerie Fine 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.