Kanebo Cosmetics Inc
⚠️ Moderate Risk
FEI: 3009159168 • Kitami-shi, Hokkai-do • JAPAN
FEI Number
3009159168
Location
Kitami-shi, Hokkai-do
Country
JAPANAddress
14 10 Nihonbashi Kayabacho 1 Cho, , Kitami-shi, Hokkai-do, Japan
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
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
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 |
|---|---|---|---|
| 8/1/2016 | 53CY07EYELASH AND EYEBROW DYE (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
| 12/4/2015 | 53LH01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | Division of Southeast Imports (DSEI) | |
| 9/30/2015 | 53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES) | 471CSTIC LBLG | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Kanebo Cosmetics Inc's FDA import refusal history?
Kanebo Cosmetics Inc (FEI: 3009159168) has 3 FDA import refusal record(s) in our database, spanning from 9/30/2015 to 8/1/2016.
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. Kanebo Cosmetics Inc's FEI number is 3009159168.
What types of violations has Kanebo Cosmetics Inc received?
Kanebo Cosmetics 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 Kanebo Cosmetics Inc come from?
All FDA import refusal data for Kanebo Cosmetics 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.