EPG Extreme Products Group
⚠️ Moderate Risk
FEI: 3011403346 • Las Vegas, NV • UNITED STATES
FEI Number
3011403346
Location
Las Vegas, NV
Country
UNITED STATESAddress
1432 Iron Hills Ln, , Las Vegas, NV, 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is EPG Extreme Products Group's FDA import refusal history?
EPG Extreme Products Group (FEI: 3011403346) has 2 FDA import refusal record(s) in our database, spanning from 4/9/2015 to 4/9/2015.
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. EPG Extreme Products Group's FEI number is 3011403346.
What types of violations has EPG Extreme Products Group received?
EPG Extreme Products Group 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 EPG Extreme Products Group come from?
All FDA import refusal data for EPG Extreme Products Group 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.