Carlos Enrique Quiroz Lizarraga
⚠️ Moderate Risk
FEI: 3003575829 • Hermosillo, Sonora • MEXICO
FEI Number
3003575829
Location
Hermosillo, Sonora
Country
MEXICOAddress
Francisco I Madero 173, , Hermosillo, Sonora, 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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/10/2002 | 24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 5/10/2002 | 24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 5/10/2002 | 24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Carlos Enrique Quiroz Lizarraga's FDA import refusal history?
Carlos Enrique Quiroz Lizarraga (FEI: 3003575829) has 3 FDA import refusal record(s) in our database, spanning from 5/10/2002 to 5/10/2002.
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. Carlos Enrique Quiroz Lizarraga's FEI number is 3003575829.
What types of violations has Carlos Enrique Quiroz Lizarraga received?
Carlos Enrique Quiroz Lizarraga 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 Carlos Enrique Quiroz Lizarraga come from?
All FDA import refusal data for Carlos Enrique Quiroz Lizarraga 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.