PRODUCTOS SELECTOS MARROKO, S.A. DE C.V.
⚠️ Moderate Risk
FEI: 3004856129 • Allende, Nuevo Leon • MEXICO
FEI Number
3004856129
Location
Allende, Nuevo Leon
Country
MEXICOAddress
Carr. Allende Cadereyta # 1201, Col. Piedras Blancas, Allende, Nuevo Leon, 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
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.
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.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/27/2010 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 7/25/2010 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 4/20/2010 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 3/24/2010 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/14/2008 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 9/29/2008 | 24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 3/19/2008 | 16JGH05SHRIMP & PRAWNS | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 11/15/2007 | 36AFH02BROWN SUGAR (SUCROSE FROM CANE) | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is PRODUCTOS SELECTOS MARROKO, S.A. DE C.V.'s FDA import refusal history?
PRODUCTOS SELECTOS MARROKO, S.A. DE C.V. (FEI: 3004856129) has 8 FDA import refusal record(s) in our database, spanning from 11/15/2007 to 7/27/2010.
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. PRODUCTOS SELECTOS MARROKO, S.A. DE C.V.'s FEI number is 3004856129.
What types of violations has PRODUCTOS SELECTOS MARROKO, S.A. DE C.V. received?
PRODUCTOS SELECTOS MARROKO, S.A. DE C.V. has been cited for 4 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 PRODUCTOS SELECTOS MARROKO, S.A. DE C.V. come from?
All FDA import refusal data for PRODUCTOS SELECTOS MARROKO, 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.