Deiman USA Corp
⚠️ Moderate Risk
FEI: 3011214803 • El Paso, TX • UNITED STATES
FEI Number
3011214803
Location
El Paso, TX
Country
UNITED STATESAddress
14300 Rudi Kuefner Dr, , El Paso, TX, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/8/2015 | 23BGB08PECAN, SHELLED | 297AFLATOXIN | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Deiman USA Corp's FDA import refusal history?
Deiman USA Corp (FEI: 3011214803) has 1 FDA import refusal record(s) in our database, spanning from 6/8/2015 to 6/8/2015.
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. Deiman USA Corp's FEI number is 3011214803.
What types of violations has Deiman USA Corp received?
Deiman USA Corp 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 Deiman USA Corp come from?
All FDA import refusal data for Deiman USA Corp 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.