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PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3004790493 • Zapopan, Jalisco • MEXICO

FEI

FEI Number

3004790493

📍

Location

Zapopan, Jalisco

🇲🇽

Country

MEXICO
🏢

Address

Calle Industria Electrica 2373, Industrial Zapopan Norte, Zapopan, Jalisco, Mexico

Moderate Risk

FDA Import Risk Assessment

35.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
11/18/2021
Latest Refusal
10/1/2021
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
22.3×30%
Recency
2.2×20%
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).

2742×

COLOR LBLG

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

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
11/18/2021
33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
11/18/2021
33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Division of Southwest Imports (DSWI)
10/1/2021
33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
256INCONSPICU
274COLOR LBLG
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V.'s FDA import refusal history?

PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V. (FEI: 3004790493) has 3 FDA import refusal record(s) in our database, spanning from 10/1/2021 to 11/18/2021.

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. PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V.'s FEI number is 3004790493.

What types of violations has PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V. received?

PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V. 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 PROCESADORA CONFITERA DE MEXICO, S.A. DE C.V. come from?

All FDA import refusal data for PROCESADORA CONFITERA DE MEXICO, 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.