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HARPER LG DE LEON, S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3004287158 • Leon, Guanajuato • MEXICO

FEI

FEI Number

3004287158

📍

Location

Leon, Guanajuato

🇲🇽

Country

MEXICO
🏢

Address

Alud 304 Penitas, , Leon, Guanajuato, Mexico

Moderate Risk

FDA Import Risk Assessment

30.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
11/9/2004
Latest Refusal
11/9/2004
Earliest Refusal

Score Breakdown

Violation Severity
50.8×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

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).

2743×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2182×

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.

3202×

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.

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.

Refusal History

DateProductViolationsDivision
11/9/2004
71EYY99ANIMAL WASTE FEED PRODUCTS, N.E.C.
11UNSAFE COL
274COLOR LBLG
Southwest Import District Office (SWI-DO)
11/9/2004
71EYY99ANIMAL WASTE FEED PRODUCTS, N.E.C.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
328USUAL NAME
Southwest Import District Office (SWI-DO)
11/9/2004
71EYY99ANIMAL WASTE FEED PRODUCTS, N.E.C.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
328USUAL NAME
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is HARPER LG DE LEON, S.A. DE C.V.'s FDA import refusal history?

HARPER LG DE LEON, S.A. DE C.V. (FEI: 3004287158) has 3 FDA import refusal record(s) in our database, spanning from 11/9/2004 to 11/9/2004.

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. HARPER LG DE LEON, S.A. DE C.V.'s FEI number is 3004287158.

What types of violations has HARPER LG DE LEON, S.A. DE C.V. received?

HARPER LG DE LEON, S.A. DE C.V. 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 HARPER LG DE LEON, S.A. DE C.V. come from?

All FDA import refusal data for HARPER LG DE LEON, S.A. DE C.V. 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.