Serafin Monteon Parra
⚠️ Moderate Risk
FEI: 3009700104 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3009700104
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Av Rio Churubusco 1015, Col. Central De Abasto, Iztapalapa, Ciudad De Mexico, Ciudad de Mexico, 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/5/2012 | 21XGD14TAMARIND (SUBTROPICAL/TROPICAL FRUIT PULP) | 249FILTHY | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Serafin Monteon Parra's FDA import refusal history?
Serafin Monteon Parra (FEI: 3009700104) has 1 FDA import refusal record(s) in our database, spanning from 11/5/2012 to 11/5/2012.
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. Serafin Monteon Parra's FEI number is 3009700104.
What types of violations has Serafin Monteon Parra received?
Serafin Monteon Parra 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 Serafin Monteon Parra come from?
All FDA import refusal data for Serafin Monteon Parra 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.