Tellez Nava Judith
⚠️ Moderate Risk
FEI: 3010237785 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3010237785
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Calle 12 # 327, Col.Leyes De Reforma 1a; Otro Leyes De Reforma 1ra. Seccion, 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
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 |
|---|---|---|---|
| 4/25/2016 | 24FHC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 2/29/2016 | 24FHC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 2/16/2016 | 24FFC13SERRANO PEPPER, HOT (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Tellez Nava Judith's FDA import refusal history?
Tellez Nava Judith (FEI: 3010237785) has 3 FDA import refusal record(s) in our database, spanning from 2/16/2016 to 4/25/2016.
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. Tellez Nava Judith's FEI number is 3010237785.
What types of violations has Tellez Nava Judith received?
Tellez Nava Judith 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 Tellez Nava Judith come from?
All FDA import refusal data for Tellez Nava Judith 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.