Soledad Laura Aranda Dominguez
⚠️ Moderate Risk
FEI: 3009639027 • Iguala • MEXICO
FEI Number
3009639027
Location
Iguala
Country
MEXICOAddress
Arcelia Calle 18 Sin Numero, , Iguala, , 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
Frequently Asked Questions
What is Soledad Laura Aranda Dominguez's FDA import refusal history?
Soledad Laura Aranda Dominguez (FEI: 3009639027) has 2 FDA import refusal record(s) in our database, spanning from 7/7/2014 to 12/21/2015.
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. Soledad Laura Aranda Dominguez's FEI number is 3009639027.
What types of violations has Soledad Laura Aranda Dominguez received?
Soledad Laura Aranda Dominguez 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 Soledad Laura Aranda Dominguez come from?
All FDA import refusal data for Soledad Laura Aranda Dominguez 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.