Del Laboratories Cda Inc.
⚠️ Moderate Risk
FEI: 3003339473 • Barrie, ON • CANADA
FEI Number
3003339473
Location
Barrie, ON
Country
CANADAAddress
316 Bayview Dr, , Barrie, 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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/26/2004 | 53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 4/26/2004 | 53GK05LIPSTICK (MAKEUP PREPARATIONS, NOT FOR EYES) | 473LABELING | New York District Office (NYK-DO) |
| 4/26/2004 | 53CG99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | New York District Office (NYK-DO) | |
| 4/26/2004 | 53CG99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 11UNSAFE COL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Del Laboratories Cda Inc.'s FDA import refusal history?
Del Laboratories Cda Inc. (FEI: 3003339473) has 4 FDA import refusal record(s) in our database, spanning from 4/26/2004 to 4/26/2004.
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. Del Laboratories Cda Inc.'s FEI number is 3003339473.
What types of violations has Del Laboratories Cda Inc. received?
Del Laboratories Cda Inc. has been cited for 3 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 Del Laboratories Cda Inc. come from?
All FDA import refusal data for Del Laboratories Cda 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.