Deiman, S.A. de C.V.
⚠️ Moderate Risk
FEI: 3004483157 • Mexico City, Distrito Federal • MEXICO
FEI Number
3004483157
Location
Mexico City, Distrito Federal
Country
MEXICOAddress
San Antonio Industrial Park 320, Acatl Street; Azcapotzalco, Mexico City, Distrito Federal, 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
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).
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)).
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
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.
COLORLABEL
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 35AFT01GELATIN, FLAVORED | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT04VANILLA (VANILLIN) IMITATION FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT04VANILLA (VANILLIN) IMITATION FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT03IMITATION NUT FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT03IMITATION NUT FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT04VANILLA (VANILLIN) IMITATION FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT03IMITATION NUT FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT99IMITATION FLAVOR, N.E.C. | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT03IMITATION NUT FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 28MGT03IMITATION NUT FLAVOR | 473LABELING | Division of Southwest Imports (DSWI) |
| 2/7/2018 | 45KY99FLAVOR ENHANCERS (FOOD ADDITIVES FOR HUMAN USE) | 328USUAL NAME | Division of Southwest Imports (DSWI) |
| 5/4/2017 | 50AHY01COLOR FOR FOODS, DRUGS AND COSMETICS (FD&C) (CERTIFIED) | Division of Southwest Imports (DSWI) | |
| 4/3/2013 | 50BGB01COLOR FOR FOOD (NOT CERTIFIED) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 4/3/2013 | 50BGB01COLOR FOR FOOD (NOT CERTIFIED) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 6/9/2011 | 50ACT01COLOR FOR FOODS, DRUGS AND COSMETICS (FD&C) (CERTIFIED) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 12/6/2010 | 50AHT01COLOR FOR FOODS, DRUGS AND COSMETICS (FD&C) (CERTIFIED) | Southwest Import District Office (SWI-DO) | |
| 12/6/2010 | 50AHT01COLOR FOR FOODS, DRUGS AND COSMETICS (FD&C) (CERTIFIED) | Southwest Import District Office (SWI-DO) | |
| 1/20/2010 | 35AGT01GELATIN, FLAVORED | 324NO ENGLISH | Southwest Import District Office (SWI-DO) |
| 1/20/2010 | 35AGT01GELATIN, FLAVORED | 324NO ENGLISH | Southwest Import District Office (SWI-DO) |
| 9/19/2008 | 45LH99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 8/11/2008 | 45LH99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
| 8/21/2006 | 50BGY01COLOR FOR FOOD (NOT CERTIFIED) | 11UNSAFE COL | Cincinnati District Office (CIN-DO) |
| 6/28/2005 | 45LH99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | 328USUAL NAME | New Orleans District Office (NOL-DO) |
| 6/28/2005 | 45LH99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Deiman, S.A. de C.V.'s FDA import refusal history?
Deiman, S.A. de C.V. (FEI: 3004483157) has 38 FDA import refusal record(s) in our database, spanning from 6/28/2005 to 2/7/2018.
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. Deiman, S.A. de C.V.'s FEI number is 3004483157.
What types of violations has Deiman, S.A. de C.V. received?
Deiman, S.A. de C.V. has been cited for 7 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 Deiman, S.A. de C.V. come from?
All FDA import refusal data for Deiman, 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.