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North American Impex Inc

⚠️ Moderate Risk

FEI: 1000354164 • Markham, Ontario • CANADA

FEI

FEI Number

1000354164

📍

Location

Markham, Ontario

🇨🇦

Country

CANADA
🏢

Address

600 Hood Rd, , Markham, Ontario, Canada

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

11
Total Refusals
11
Unique Violations
12/23/2008
Latest Refusal
8/26/2002
Earliest Refusal

Score Breakdown

Violation Severity
56.5×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
17.4×10%
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

2184×

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.

2604×

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.

113×

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).

643×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

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.

2512×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

20401×

SULFITELBL

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.

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.

3211×

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.

3201×

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.

Refusal History

DateProductViolationsDivision
12/23/2008
21BGT99MIXED FRUIT, DRIED OR PASTE, N.E.C.,
11UNSAFE COL
2040SULFITELBL
218LIST INGRE
New York District Office (NYK-DO)
12/12/2008
21BGT99MIXED FRUIT, DRIED OR PASTE, N.E.C.,
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
8/19/2008
23HGT99MIXED NUTS, SHELLED, N.E.C.
260FALSE
Detroit District Office (DET-DO)
8/19/2008
23HGT99MIXED NUTS, SHELLED, N.E.C.
260FALSE
Detroit District Office (DET-DO)
8/19/2008
23HGT99MIXED NUTS, SHELLED, N.E.C.
260FALSE
Detroit District Office (DET-DO)
8/19/2008
23HGT99MIXED NUTS, SHELLED, N.E.C.
260FALSE
Detroit District Office (DET-DO)
8/19/2008
21BGT99MIXED FRUIT, DRIED OR PASTE, N.E.C.,
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
64YELLOW #5
Detroit District Office (DET-DO)
8/19/2008
21BGT99MIXED FRUIT, DRIED OR PASTE, N.E.C.,
11UNSAFE COL
218LIST INGRE
276PRESRV LBL
64YELLOW #5
Detroit District Office (DET-DO)
11/3/2003
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
251POISONOUS
New York District Office (NYK-DO)
10/15/2003
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
251POISONOUS
New York District Office (NYK-DO)
8/26/2002
33LFT14TAFFY (TOFFEE), KISSES CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
64YELLOW #5
New York District Office (NYK-DO)

Frequently Asked Questions

What is North American Impex Inc's FDA import refusal history?

North American Impex Inc (FEI: 1000354164) has 11 FDA import refusal record(s) in our database, spanning from 8/26/2002 to 12/23/2008.

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. North American Impex Inc's FEI number is 1000354164.

What types of violations has North American Impex Inc received?

North American Impex Inc has been cited for 11 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 North American Impex Inc come from?

All FDA import refusal data for North American Impex Inc 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.