LA VISTA ALIMENTOS SA DE CV
⚠️ High Risk
FEI: 3015163202 • Zamora De Hidalgo, Michoacan de Ocampo • MEXICO
FEI Number
3015163202
Location
Zamora De Hidalgo, Michoacan de Ocampo
Country
MEXICOAddress
Calle Camino Del Jerico # 1012, Fracc. Colonia, Zamora, Zamora De Hidalgo, 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:
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/23/2024 | 20AHD14STRAWBERRIES (BERRY) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 2/18/2020 | 20FHD14STRAWBERRIES (BERRY PUREES) | Division of Southwest Imports (DSWI) | |
| 6/12/2017 | 20FGD14STRAWBERRIES (BERRY PUREES) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 5/10/2017 | 20FFS14STRAWBERRIES (BERRY PUREES) | Division of Southwest Imports (DSWI) | |
| 7/21/2015 | 20FFD14STRAWBERRIES (BERRY PUREES) | Southwest Import District Office (SWI-DO) | |
| 3/2/2010 | 21RHD04GUAVA (SUBTROPICAL AND TROPICAL FRUIT PUREES) | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 4/21/2006 | 20AHD14STRAWBERRIES (BERRY) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 12/27/2005 | 21SHT14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 12/27/2005 | 22AHT01CANTALOUPE (VINE FRUIT) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is LA VISTA ALIMENTOS SA DE CV's FDA import refusal history?
LA VISTA ALIMENTOS SA DE CV (FEI: 3015163202) has 9 FDA import refusal record(s) in our database, spanning from 12/27/2005 to 2/23/2024.
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. LA VISTA ALIMENTOS SA DE CV's FEI number is 3015163202.
What types of violations has LA VISTA ALIMENTOS SA DE CV received?
LA VISTA ALIMENTOS SA DE CV has been cited for 6 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 LA VISTA ALIMENTOS SA DE CV come from?
All FDA import refusal data for LA VISTA ALIMENTOS SA DE CV 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.