HERMANOS TEMIS
⚠️ High Risk
FEI: 3007909914 • Ixhuatlan, Veracruz • MEXICO
FEI Number
3007909914
Location
Ixhuatlan, Veracruz
Country
MEXICOAddress
Cale Concorida, Col Centro, Ixhuatlan, Veracruz, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 |
|---|---|---|---|
| 2/10/2012 | 20GFB05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 2/6/2012 | 20GFB05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 2/6/2012 | 20GFB05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 1/30/2012 | 20GFC05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 1/12/2012 | 20GFC05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 11/14/2011 | 20GFB05LIME (CITRUS) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is HERMANOS TEMIS's FDA import refusal history?
HERMANOS TEMIS (FEI: 3007909914) has 6 FDA import refusal record(s) in our database, spanning from 11/14/2011 to 2/10/2012.
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. HERMANOS TEMIS's FEI number is 3007909914.
What types of violations has HERMANOS TEMIS received?
HERMANOS TEMIS 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 HERMANOS TEMIS come from?
All FDA import refusal data for HERMANOS TEMIS 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.