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Kobi International Company

⚠️ Moderate Risk

FEI: 3003715061 • Toronto, ON • CANADA

FEI

FEI Number

3003715061

📍

Location

Toronto, ON

🇨🇦

Country

CANADA
🏢

Address

40 King Street, , Toronto, ON, Canada

Moderate Risk

FDA Import Risk Assessment

34.2
LowModerateHighCritical

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

Statistics

7
Total Refusals
5
Unique Violations
10/7/2003
Latest Refusal
10/7/2003
Earliest Refusal

Score Breakdown

Violation Severity
42.9×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

4737×

LABELING

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

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.

111×

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).

2181×

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.

2761×

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.

Refusal History

DateProductViolationsDivision
10/7/2003
29BGT50SOFT DRINK, COLA, CARBONATED
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BHT50SOFT DRINK, COLA, CARBONATED
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BHT50SOFT DRINK, COLA, CARBONATED
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BHT50SOFT DRINK, COLA, CARBONATED
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BGT50SOFT DRINK, COLA, CARBONATED
276PRESRV LBL
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BHT50SOFT DRINK, COLA, CARBONATED
218LIST INGRE
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
10/7/2003
29BGT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Kobi International Company's FDA import refusal history?

Kobi International Company (FEI: 3003715061) has 7 FDA import refusal record(s) in our database, spanning from 10/7/2003 to 10/7/2003.

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. Kobi International Company's FEI number is 3003715061.

What types of violations has Kobi International Company received?

Kobi International Company 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 Kobi International Company come from?

All FDA import refusal data for Kobi International Company 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.