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Kerry Inc.

⚠️ Moderate Risk

FEI: 3004290121 • Irapuato, Guanajuato • MEXICO

FEI

FEI Number

3004290121

📍

Location

Irapuato, Guanajuato

🇲🇽

Country

MEXICO
🏢

Address

Carretera Panamericana Km 11.2, Ciudad Industrial Ciudad Industrial, Irapuato, Guanajuato, Mexico

Moderate Risk

FDA Import Risk Assessment

41.1
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
2/23/2011
Latest Refusal
4/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
72.0×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
11.4×10%
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

2496×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

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.

3242×

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
2/23/2011
28CHH99NATURAL EXTRACT OR FLAVOR, N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)
8/28/2006
09CGH99MILK AND CREAM, N.E.C.
321LACKS N/C
324NO ENGLISH
Southwest Import District Office (SWI-DO)
8/28/2006
09CGH99MILK AND CREAM, N.E.C.
321LACKS N/C
Southwest Import District Office (SWI-DO)
7/20/2006
21RGY14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT PUREES)
249FILTHY
Southwest Import District Office (SWI-DO)
11/4/2005
21TGH14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
11/3/2005
21TGH14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
5/13/2004
21TYN14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
4/14/2003
21TYN14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
4/14/2003
21TYN14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Kerry Inc.'s FDA import refusal history?

Kerry Inc. (FEI: 3004290121) has 9 FDA import refusal record(s) in our database, spanning from 4/14/2003 to 2/23/2011.

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. Kerry Inc.'s FEI number is 3004290121.

What types of violations has Kerry Inc. received?

Kerry Inc. 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 Kerry Inc. come from?

All FDA import refusal data for Kerry 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.