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Antoun Sani

⚠️ Moderate Risk

FEI: 3002978351 • Laval, Quebec • CANADA

FEI

FEI Number

3002978351

📍

Location

Laval, Quebec

🇨🇦

Country

CANADA
🏢

Address

1680 Jordan Ave, , Laval, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

35.9
LowModerateHighCritical

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

Statistics

8
Total Refusals
10
Unique Violations
8/8/2005
Latest Refusal
5/9/2003
Earliest Refusal

Score Breakdown

Violation Severity
54.3×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
35.5×10%
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

115×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2183×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

4823×

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.

3282×

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.

2762×

PRESRV LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.

3212×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4731×

LABELING

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

2561×

INCONSPICU

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
8/8/2005
23GHT01NON-STANDARDIZED MIXED NUTS, IN SHELL
482NUTRIT LBL
New York District Office (NYK-DO)
8/8/2005
25YHT99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
321LACKS N/C
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/8/2005
21BFT99MIXED FRUIT, DRIED OR PASTE, N.E.C.,
11UNSAFE COL
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
2/11/2005
03RGT25PASTRY (OTHER THAN FRUIT OR JELLY FILLED) WITHOUT CUSTARD OR CREAM FILLING
256INCONSPICU
New York District Office (NYK-DO)
12/1/2004
03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C.
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
11/23/2004
03RGT25PASTRY (OTHER THAN FRUIT OR JELLY FILLED) WITHOUT CUSTARD OR CREAM FILLING
11UNSAFE COL
328USUAL NAME
New York District Office (NYK-DO)
11/23/2004
03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING
11UNSAFE COL
New York District Office (NYK-DO)
5/9/2003
03AGT14CROISSANT BREAD/ROLLS
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Antoun Sani's FDA import refusal history?

Antoun Sani (FEI: 3002978351) has 8 FDA import refusal record(s) in our database, spanning from 5/9/2003 to 8/8/2005.

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. Antoun Sani's FEI number is 3002978351.

What types of violations has Antoun Sani received?

Antoun Sani has been cited for 10 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 Antoun Sani come from?

All FDA import refusal data for Antoun Sani 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.