SunOpta MX S.A. de C.V.
⚠️ High Risk
FEI: 3009451028 • Jacona De Plancarte, Michoacan de Ocampo • MEXICO
FEI Number
3009451028
Location
Jacona De Plancarte, Michoacan de Ocampo
Country
MEXICOAddress
Calle La Haciendita # 8, Fracc. Los Laureles, Jacona, Jacona De Plancarte, Michoacan de Ocampo, 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 |
|---|---|---|---|
| 10/31/2023 | 20AGD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 8/22/2023 | 20AGD13RASPBERRIES, RED (BERRY) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 3/28/2017 | 20AFD14STRAWBERRIES (BERRY) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 4/11/2014 | 20AGD14STRAWBERRIES (BERRY) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is SunOpta MX S.A. de C.V.'s FDA import refusal history?
SunOpta MX S.A. de C.V. (FEI: 3009451028) has 4 FDA import refusal record(s) in our database, spanning from 4/11/2014 to 10/31/2023.
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. SunOpta MX S.A. de C.V.'s FEI number is 3009451028.
What types of violations has SunOpta MX S.A. de C.V. received?
SunOpta MX S.A. de C.V. 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 SunOpta MX S.A. de C.V. come from?
All FDA import refusal data for SunOpta MX S.A. de C.V. 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.