PRODUCTOS ALSEF S.A. DE C.V.
⚠️ High Risk
FEI: 3008007885 • Ciudad General Escobedo, Nuevo Leon • MEXICO
FEI Number
3008007885
Location
Ciudad General Escobedo, Nuevo Leon
Country
MEXICOAddress
Calle Industria Electrica 1, Col. Parque Industrial Escobedo, Gral. Escobedo, Ciudad General Escobedo, Nuevo Leon, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/22/2014 | 07BGT02CORN CHIPS, FRIED | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 4/22/2014 | 07BGT02CORN CHIPS, FRIED | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 3/18/2014 | 07YHB99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C. | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 2/10/2014 | 07BGT02CORN CHIPS, FRIED | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is PRODUCTOS ALSEF S.A. DE C.V.'s FDA import refusal history?
PRODUCTOS ALSEF S.A. DE C.V. (FEI: 3008007885) has 4 FDA import refusal record(s) in our database, spanning from 2/10/2014 to 4/22/2014.
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 ALSEF S.A. DE C.V.'s FEI number is 3008007885.
What types of violations has PRODUCTOS ALSEF S.A. DE C.V. received?
PRODUCTOS ALSEF S.A. DE C.V. has been cited for 1 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 ALSEF S.A. DE C.V. come from?
All FDA import refusal data for PRODUCTOS ALSEF 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.