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TopDay S.A. de C.V.

⚠️ Moderate Risk

FEI: 3010280682 • Guadalajara, JAL • MEXICO

FEI

FEI Number

3010280682

📍

Location

Guadalajara, JAL

🇲🇽

Country

MEXICO
🏢

Address

Francisco Villa No. 984, Colonia Agua Blanca Industrial, Guadalajara, JAL, Mexico

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
10/8/2013
Latest Refusal
10/8/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

3243×

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)).

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.

33002×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

Refusal History

DateProductViolationsDivision
10/8/2013
37JHT03CHILI SAUCE
324NO ENGLISH
Southwest Import District Office (SWI-DO)
10/8/2013
07AGT99BAKED SNACK FOOD, N.E.C.
218LIST INGRE
324NO ENGLISH
3300ALLERGEN
Southwest Import District Office (SWI-DO)
10/8/2013
07AGT99BAKED SNACK FOOD, N.E.C.
218LIST INGRE
324NO ENGLISH
3300ALLERGEN
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is TopDay S.A. de C.V.'s FDA import refusal history?

TopDay S.A. de C.V. (FEI: 3010280682) has 3 FDA import refusal record(s) in our database, spanning from 10/8/2013 to 10/8/2013.

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. TopDay S.A. de C.V.'s FEI number is 3010280682.

What types of violations has TopDay S.A. de C.V. received?

TopDay 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 TopDay S.A. de C.V. come from?

All FDA import refusal data for TopDay 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.