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Carolina Suarez Suarez

⚠️ Moderate Risk

FEI: 3010121216 • Xico, Veracruz • MEXICO

FEI

FEI Number

3010121216

📍

Location

Xico, Veracruz

🇲🇽

Country

MEXICO
🏢

Address

Calle Xico Coatepec Km 1, , Xico, Veracruz, Mexico

Moderate Risk

FDA Import Risk Assessment

25.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
10/26/2016
Latest Refusal
3/3/2011
Earliest Refusal

Score Breakdown

Violation Severity
42.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
7.1×10%
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

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3191×

WRONG IDEN

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 as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.

3241×

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
10/26/2016
28CHT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), NATURAL EXTRACT OR FLAVOR (SPICE)
260FALSE
319WRONG IDEN
Southwest Import District Office (SWI-DO)
1/19/2012
37KHT18MOLE PASTE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
1/19/2012
37KHT18MOLE PASTE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
3/3/2011
37KHT99PASTES, N.E.C.
324NO ENGLISH
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Carolina Suarez Suarez's FDA import refusal history?

Carolina Suarez Suarez (FEI: 3010121216) has 4 FDA import refusal record(s) in our database, spanning from 3/3/2011 to 10/26/2016.

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. Carolina Suarez Suarez's FEI number is 3010121216.

What types of violations has Carolina Suarez Suarez received?

Carolina Suarez Suarez has been cited for 4 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 Carolina Suarez Suarez come from?

All FDA import refusal data for Carolina Suarez Suarez 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.