INDUSTRIA DE REFRESCOS
⚠️ Moderate Risk
FEI: 3014418056 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3014418056
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Avenida Santa Fe 485, Col. Contadero, Cuajimalpa De Morelos, Ciudad De Mexico, Ciudad de Mexico, Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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)).
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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)).
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/3/2022 | 29BCT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED | Division of Southwest Imports (DSWI) | |
| 7/28/2020 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | Division of Southwest Imports (DSWI) | |
| 2/13/2020 | 29BCE02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED | Division of Southwest Imports (DSWI) | |
| 2/5/2020 | 29BCY50SOFT DRINK, COLA, CARBONATED | Division of Southwest Imports (DSWI) | |
| 11/13/2019 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | 482NUTRIT LBL | Division of Northeast Imports (DNEI) |
| 11/13/2019 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
| 11/13/2019 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is INDUSTRIA DE REFRESCOS's FDA import refusal history?
INDUSTRIA DE REFRESCOS (FEI: 3014418056) has 7 FDA import refusal record(s) in our database, spanning from 11/13/2019 to 1/3/2022.
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. INDUSTRIA DE REFRESCOS's FEI number is 3014418056.
What types of violations has INDUSTRIA DE REFRESCOS received?
INDUSTRIA DE REFRESCOS 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 INDUSTRIA DE REFRESCOS come from?
All FDA import refusal data for INDUSTRIA DE REFRESCOS 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.