Grupo Alinorsa S.A. de C.V
⚠️ Moderate Risk
FEI: 2000029346 • Monterrey, Nuevo Leon • MEXICO
FEI Number
2000029346
Location
Monterrey, Nuevo Leon
Country
MEXICOAddress
Calle Keramos 210-7, Col. Del Prado, Monterrey, Monterrey, 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
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/9/2008 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 4/9/2008 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 1/9/2008 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 1/9/2008 | 27YCE06PEPPER SAUCE (HOT, MILD, ETC.) | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Grupo Alinorsa S.A. de C.V's FDA import refusal history?
Grupo Alinorsa S.A. de C.V (FEI: 2000029346) has 4 FDA import refusal record(s) in our database, spanning from 1/9/2008 to 4/9/2008.
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 Alinorsa S.A. de C.V's FEI number is 2000029346.
What types of violations has Grupo Alinorsa S.A. de C.V received?
Grupo Alinorsa 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 Grupo Alinorsa S.A. de C.V come from?
All FDA import refusal data for Grupo Alinorsa 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.