NUGENESIS NAILS
✅ Low Risk
FEI: 3012080114 • Concord, ON • CANADA
FEI Number
3012080114
Location
Concord, ON
Country
CANADAAddress
328 North Rivermede Rd, , Concord, ON, Canada
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/12/2016 | 53HY05NAIL POLISH AND ENAMEL (MANICURING PREPARATIONS) | 475COSMETLBLG | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is NUGENESIS NAILS's FDA import refusal history?
NUGENESIS NAILS (FEI: 3012080114) has 1 FDA import refusal record(s) in our database, spanning from 10/12/2016 to 10/12/2016.
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. NUGENESIS NAILS's FEI number is 3012080114.
What types of violations has NUGENESIS NAILS received?
NUGENESIS NAILS 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 NUGENESIS NAILS come from?
All FDA import refusal data for NUGENESIS NAILS 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.