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COMPANIA MAYORISTA DE PRODUCTOSS.A

⚠️ Moderate Risk

FEI: 3023417137 • San Miguel Petapa • GUATEMALA

FEI

FEI Number

3023417137

📍

Location

San Miguel Petapa

🇬🇹

Country

GUATEMALA
🏢

Address

14 Calle B 12-15, Zona7 Petapa 2, , San Miguel Petapa, , Guatemala

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

6
Total Refusals
8
Unique Violations
6/25/2024
Latest Refusal
3/31/2023
Earliest Refusal

Score Breakdown

Violation Severity
39.4×40%
Refusal Volume
31.3×30%
Recency
54.6×20%
Frequency
48.5×10%
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

4825×

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.

2563×

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)).

3203×

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.

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)).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

2181×

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.

Refusal History

DateProductViolationsDivision
6/25/2024
07BYY02CORN CHIPS, FRIED
256INCONSPICU
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)
6/25/2024
07BYY02CORN CHIPS, FRIED
256INCONSPICU
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)
6/25/2024
07BYY02CORN CHIPS, FRIED
256INCONSPICU
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)
7/14/2023
20KYI06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES
218LIST INGRE
473LABELING
62NEEDS FCE
83NO PROCESS
Division of Southwest Imports (DSWI)
3/31/2023
20KYY06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/31/2023
20KYY06ORANGE, CITRUS FRUIT JUICES OR CONCENTRATES
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is COMPANIA MAYORISTA DE PRODUCTOSS.A's FDA import refusal history?

COMPANIA MAYORISTA DE PRODUCTOSS.A (FEI: 3023417137) has 6 FDA import refusal record(s) in our database, spanning from 3/31/2023 to 6/25/2024.

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. COMPANIA MAYORISTA DE PRODUCTOSS.A's FEI number is 3023417137.

What types of violations has COMPANIA MAYORISTA DE PRODUCTOSS.A received?

COMPANIA MAYORISTA DE PRODUCTOSS.A has been cited for 8 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 COMPANIA MAYORISTA DE PRODUCTOSS.A come from?

All FDA import refusal data for COMPANIA MAYORISTA DE PRODUCTOSS.A 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.