ImportRefusal LogoImportRefusal

JOSUE DE LA FUENTES DOMINGUEZ

⚠️ High Risk

FEI: 3019665308 • Zapotitan De Hidalgo, Jalisco • MEXICO

FEI

FEI Number

3019665308

📍

Location

Zapotitan De Hidalgo, Jalisco

🇲🇽

Country

MEXICO
🏢

Address

Calle Emiliano Zapata No. 33, Col. Zapotitan De Hidalgo, Jocotepec, Zapotitan De Hidalgo, Jalisco, Mexico

High Risk

FDA Import Risk Assessment

56.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
3
Unique Violations
2/10/2023
Latest Refusal
1/12/2022
Earliest Refusal

Score Breakdown

Violation Severity
83.3×40%
Refusal Volume
35.3×30%
Recency
27.4×20%
Frequency
74.1×10%
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

2416×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

38862×

FSVP VIO

The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.

2561×

INCONSPICU

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
2/10/2023
24TFC73NOPAL CACTUS (LEAF & STEM VEGETABLE)
3886FSVP VIO
Division of Southwest Imports (DSWI)
2/10/2023
24TGC08CABBAGE (LEAF & STEM VEGETABLE)
3886FSVP VIO
Division of Southwest Imports (DSWI)
6/10/2022
25JFC01CARROT (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
2/17/2022
25JFC01CARROT (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
1/26/2022
24TGC46CILANTRO (LEAF & STEM VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
1/25/2022
25JGC01CARROT (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
1/25/2022
25JGC01CARROT (ROOT & TUBER VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
1/12/2022
25JGC01CARROT (ROOT & TUBER VEGETABLE)
241PESTICIDE
256INCONSPICU
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is JOSUE DE LA FUENTES DOMINGUEZ's FDA import refusal history?

JOSUE DE LA FUENTES DOMINGUEZ (FEI: 3019665308) has 8 FDA import refusal record(s) in our database, spanning from 1/12/2022 to 2/10/2023.

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. JOSUE DE LA FUENTES DOMINGUEZ's FEI number is 3019665308.

What types of violations has JOSUE DE LA FUENTES DOMINGUEZ received?

JOSUE DE LA FUENTES DOMINGUEZ 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 JOSUE DE LA FUENTES DOMINGUEZ come from?

All FDA import refusal data for JOSUE DE LA FUENTES DOMINGUEZ 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.