Ebara-Udylite Co Ltd
⚠️ Moderate Risk
FEI: 3001801327 • Tokyo • 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
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/11/2003 | 37JEN99SAUCES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/11/2003 | 37JCT99SAUCES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 9/12/2002 | 37JHT99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 9/11/2002 | 37JHT99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Ebara-Udylite Co Ltd's FDA import refusal history?
Ebara-Udylite Co Ltd (FEI: 3001801327) has 4 FDA import refusal record(s) in our database, spanning from 9/11/2002 to 2/11/2003.
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. Ebara-Udylite Co Ltd's FEI number is 3001801327.
What types of violations has Ebara-Udylite Co Ltd received?
Ebara-Udylite Co Ltd has been cited for 2 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 Ebara-Udylite Co Ltd come from?
All FDA import refusal data for Ebara-Udylite 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.