Montes de Molina SPA
⚠️ High Risk
FEI: 3010614994 • Molina, Septima Region del Maule • CHILE
FEI Number
3010614994
Location
Molina, Septima Region del Maule
Country
CHILEAddress
Vina El Carmen Lote 2 A, , Molina, Septima Region del Maule, Chile
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 |
|---|---|---|---|
| 6/20/2025 | 20AFD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Northern Border Imports (DNBI) |
| 6/26/2024 | 20AGD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 6/26/2023 | 20AGD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 5/2/2023 | 20AGD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is Montes de Molina SPA's FDA import refusal history?
Montes de Molina SPA (FEI: 3010614994) has 4 FDA import refusal record(s) in our database, spanning from 5/2/2023 to 6/20/2025.
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. Montes de Molina SPA's FEI number is 3010614994.
What types of violations has Montes de Molina SPA received?
Montes de Molina SPA 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 Montes de Molina SPA come from?
All FDA import refusal data for Montes de Molina SPA 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.