Luis Alberto Alcaraz Lopez
⚠️ Moderate Risk
FEI: 3001743733 • Guadalajara, Jalisco • MEXICO
FEI Number
3001743733
Location
Guadalajara, Jalisco
Country
MEXICOAddress
Rublo No. 3960 S.L., , Guadalajara, Jalisco, 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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
Frequently Asked Questions
What is Luis Alberto Alcaraz Lopez's FDA import refusal history?
Luis Alberto Alcaraz Lopez (FEI: 3001743733) has 2 FDA import refusal record(s) in our database, spanning from 3/11/2002 to 4/1/2002.
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. Luis Alberto Alcaraz Lopez's FEI number is 3001743733.
What types of violations has Luis Alberto Alcaraz Lopez received?
Luis Alberto Alcaraz Lopez 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 Luis Alberto Alcaraz Lopez come from?
All FDA import refusal data for Luis Alberto Alcaraz Lopez 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.