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Symbio Import Export

✅ Low Risk

FEI: 3003213559 • Montreal Nord, QUEBEC • CANADA

FEI

FEI Number

3003213559

📍

Location

Montreal Nord, QUEBEC

🇨🇦

Country

CANADA
🏢

Address

10741 Racette St, , Montreal Nord, QUEBEC, Canada

Low Risk

FDA Import Risk Assessment

24.4
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

4
Total Refusals
3
Unique Violations
9/2/2004
Latest Refusal
4/21/2003
Earliest Refusal

Score Breakdown

Violation Severity
34.3×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
29.2×10%
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

3203×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

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.

3241×

NO ENGLISH

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)).

Refusal History

DateProductViolationsDivision
9/2/2004
26ACE09VIRGIN OLIVE OIL, CRUDE
320LACKS FIRM
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
9/2/2004
26ACE09VIRGIN OLIVE OIL, CRUDE
320LACKS FIRM
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
9/2/2004
26CHY04OLIVE OIL, REFINED, SINGLE INGREDIENT
320LACKS FIRM
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
4/21/2003
02FGT04SEMOLINA, WHEAT
324NO ENGLISH
New England District Office (NWE-DO)

Frequently Asked Questions

What is Symbio Import Export's FDA import refusal history?

Symbio Import Export (FEI: 3003213559) has 4 FDA import refusal record(s) in our database, spanning from 4/21/2003 to 9/2/2004.

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. Symbio Import Export's FEI number is 3003213559.

What types of violations has Symbio Import Export received?

Symbio Import Export 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 Symbio Import Export come from?

All FDA import refusal data for Symbio Import Export 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.