Percara Enterprises Inc
⚠️ Moderate Risk
FEI: 3004932876 • Burlington, ON • CANADA
FEI Number
3004932876
Location
Burlington, ON
Country
CANADAAddress
3250 Harvester Road, , Burlington, ON, Canada
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
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 |
|---|---|---|---|
| 12/8/2005 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 12/8/2005 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 12/8/2005 | 53BD02BUBBLE BATHS (BATH PREPARATIONS) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 12/8/2005 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 12/8/2005 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 475COSMETLBLG | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Percara Enterprises Inc's FDA import refusal history?
Percara Enterprises Inc (FEI: 3004932876) has 5 FDA import refusal record(s) in our database, spanning from 12/8/2005 to 12/8/2005.
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. Percara Enterprises Inc's FEI number is 3004932876.
What types of violations has Percara Enterprises Inc received?
Percara Enterprises Inc 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 Percara Enterprises Inc come from?
All FDA import refusal data for Percara Enterprises Inc 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.