GRUPO LA FLORIDA MEXICO, S.A. DE C.V.
⚠️ Moderate Risk
FEI: 3008314142 • Tlalnepantla, Mexico • MEXICO
FEI Number
3008314142
Location
Tlalnepantla, Mexico
Country
MEXICOAddress
Calzada Vallejo 1100, Parque Industrial Prado Vallejo, Tlalnepantla De Baz, Tlalnepantla, 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
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
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.
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)).
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.
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.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/22/2020 | 20CGC99BERRIES, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED, N.E.C. | 3886FSVP VIO | Division of Southwest Imports (DSWI) |
| 6/22/2020 | 33SFC01CAKE DECORATION (WITHOUT CHOCOLATE) | 3886FSVP VIO | Division of Southwest Imports (DSWI) |
| 6/22/2020 | 13BHT99CUSTARD, N.E.C. | 3886FSVP VIO | Division of Southwest Imports (DSWI) |
| 6/22/2020 | 13BHT99CUSTARD, N.E.C. | 3886FSVP VIO | Division of Southwest Imports (DSWI) |
| 1/19/2018 | 21SGI03FIG (SUBTROPICAL AND TROPICAL FRUIT) | Division of Southwest Imports (DSWI) | |
| 1/19/2018 | 25JGI17JICAMA (ROOT & TUBER VEGETABLE) | Division of Southwest Imports (DSWI) | |
| 5/18/2016 | 26EFC01OLEOMARGARINE | Division of Southwest Imports (DSWI) | |
| 9/5/2014 | 03UHT02ICING AND ICING MIXES WITH CHOCOLATE | Southwest Import District Office (SWI-DO) | |
| 7/2/2013 | 21UHT07PINEAPPLE, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is GRUPO LA FLORIDA MEXICO, S.A. DE C.V.'s FDA import refusal history?
GRUPO LA FLORIDA MEXICO, S.A. DE C.V. (FEI: 3008314142) has 9 FDA import refusal record(s) in our database, spanning from 7/2/2013 to 6/22/2020.
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. GRUPO LA FLORIDA MEXICO, S.A. DE C.V.'s FEI number is 3008314142.
What types of violations has GRUPO LA FLORIDA MEXICO, S.A. DE C.V. received?
GRUPO LA FLORIDA MEXICO, S.A. DE C.V. has been cited for 10 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 GRUPO LA FLORIDA MEXICO, S.A. DE C.V. come from?
All FDA import refusal data for GRUPO LA FLORIDA 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.