Japan Gals Co Ltd
✅ Low Risk
FEI: 3010348408 • Chuo Shikoku Chuo, Ehime • JAPAN
FEI Number
3010348408
Location
Chuo Shikoku Chuo, Ehime
Country
JAPANAddress
2 12-10, Mishima, Chuo Shikoku Chuo, Ehime, Japan
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/3/2019 | 53LY08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS) | 473LABELING | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Japan Gals Co Ltd's FDA import refusal history?
Japan Gals Co Ltd (FEI: 3010348408) has 1 FDA import refusal record(s) in our database, spanning from 9/3/2019 to 9/3/2019.
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. Japan Gals Co Ltd's FEI number is 3010348408.
What types of violations has Japan Gals Co Ltd received?
Japan Gals Co Ltd 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 Japan Gals Co Ltd come from?
All FDA import refusal data for Japan Gals Co Ltd 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.