Deisi Elizabeth Galvan Herrera
⚠️ Moderate Risk
FEI: 3011369422 • San Nicolas de los Garza, Nuevo Leon • MEXICO
FEI Number
3011369422
Location
San Nicolas de los Garza, Nuevo Leon
Country
MEXICOAddress
Avenida Los Angeles 1000 Int L296, , San Nicolas de los Garza, 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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/18/2015 | 21SFC06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT) | 9SALMONELLA | Division of Southwest Imports (DSWI) |
| 8/18/2015 | 21SFC06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT) | 9SALMONELLA | Division of Southwest Imports (DSWI) |
| 8/17/2015 | 21SFC06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT) | 9SALMONELLA | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Deisi Elizabeth Galvan Herrera's FDA import refusal history?
Deisi Elizabeth Galvan Herrera (FEI: 3011369422) has 3 FDA import refusal record(s) in our database, spanning from 8/17/2015 to 8/18/2015.
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. Deisi Elizabeth Galvan Herrera's FEI number is 3011369422.
What types of violations has Deisi Elizabeth Galvan Herrera received?
Deisi Elizabeth Galvan Herrera 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 Deisi Elizabeth Galvan Herrera come from?
All FDA import refusal data for Deisi Elizabeth Galvan Herrera 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.