Mariadelrosario Zuniga Lizarraga
⚠️ Moderate Risk
FEI: 3003902824 • Baja California Sur • MEXICO
FEI Number
3003902824
Location
Baja California Sur
Country
MEXICOAddress
Ejido La Matanza, , Baja California Sur, , 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
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/8/2004 | 24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 306INSANITARY | Southwest Import District Office (SWI-DO) |
| 3/3/2004 | 24FFB50TOMATOES (FRUIT USED AS VEGETABLE) | 306INSANITARY | Southwest Import District Office (SWI-DO) |
| 3/3/2004 | 24FFB50TOMATOES (FRUIT USED AS VEGETABLE) | 306INSANITARY | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Mariadelrosario Zuniga Lizarraga's FDA import refusal history?
Mariadelrosario Zuniga Lizarraga (FEI: 3003902824) has 3 FDA import refusal record(s) in our database, spanning from 3/3/2004 to 3/8/2004.
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. Mariadelrosario Zuniga Lizarraga's FEI number is 3003902824.
What types of violations has Mariadelrosario Zuniga Lizarraga received?
Mariadelrosario Zuniga 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 Mariadelrosario Zuniga Lizarraga come from?
All FDA import refusal data for Mariadelrosario Zuniga 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.