COMERCIALIZADORA RB. DE RL DE CV
⚠️ High Risk
FEI: 3011403994 • Culiacan Rosales, Sinaloa • MEXICO
FEI Number
3011403994
Location
Culiacan Rosales, Sinaloa
Country
MEXICOAddress
Avenida Rio Balsas Industrial Bravo 924, Col. Industrial Bravo, Culiacan, Culiacan Rosales, Sinaloa, 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
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 |
|---|---|---|---|
| 12/1/2016 | 24FFC20CUCUMBERS (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/15/2016 | 24FFC20CUCUMBERS (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/15/2016 | 24FFC20CUCUMBERS (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 11/15/2016 | 24FFC20CUCUMBERS (FRUIT USED AS VEGETABLE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is COMERCIALIZADORA RB. DE RL DE CV's FDA import refusal history?
COMERCIALIZADORA RB. DE RL DE CV (FEI: 3011403994) has 4 FDA import refusal record(s) in our database, spanning from 11/15/2016 to 12/1/2016.
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. COMERCIALIZADORA RB. DE RL DE CV's FEI number is 3011403994.
What types of violations has COMERCIALIZADORA RB. DE RL DE CV received?
COMERCIALIZADORA RB. DE RL DE CV 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 COMERCIALIZADORA RB. DE RL DE CV come from?
All FDA import refusal data for COMERCIALIZADORA RB. DE RL 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.