COBASA COMERCIALIZADORA AXIV SA DE CV
⚠️ Moderate Risk
FEI: 3010168850 • Guadalajara, Jalisco • MEXICO
FEI Number
3010168850
Location
Guadalajara, Jalisco
Country
MEXICOAddress
Camino Nacional No. 1600, Bodega 2 Y 3; Col. Mariano Otero, Guadalajara, Jalisco, 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
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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).
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.
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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/14/2018 | 33BGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), HARD, WITH COCONUT (WITHOUT CHOCOLATE) | Division of Southwest Imports (DSWI) | |
| 1/15/2015 | 33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) | |
| 5/29/2013 | 21SFC14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 8/31/2012 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 8/31/2012 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 4/18/2012 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 4/13/2012 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 4/4/2012 | 28AGC27MARJORAM, WHOLE (SPICE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is COBASA COMERCIALIZADORA AXIV SA DE CV's FDA import refusal history?
COBASA COMERCIALIZADORA AXIV SA DE CV (FEI: 3010168850) has 8 FDA import refusal record(s) in our database, spanning from 4/4/2012 to 3/14/2018.
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. COBASA COMERCIALIZADORA AXIV SA DE CV's FEI number is 3010168850.
What types of violations has COBASA COMERCIALIZADORA AXIV SA DE CV received?
COBASA COMERCIALIZADORA AXIV SA DE CV 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 COBASA COMERCIALIZADORA AXIV SA DE CV come from?
All FDA import refusal data for COBASA COMERCIALIZADORA AXIV SA DE CV 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.