Uwajima Project Ltd
⚠️ Moderate Risk
FEI: 3009273035 • Uwajima, Ehime • JAPAN
FEI Number
3009273035
Location
Uwajima, Ehime
Country
JAPANAddress
Sakashizu 94-13, , Uwajima, Ehime, 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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
MFRHACCP
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/27/2013 | 16AGD79YELLOWTAIL, AMBERJACK | 2580MFRHACCP | Los Angeles District Office (LOS-DO) |
| 8/27/2013 | 16AGN33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 8/27/2013 | 16AGN33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Uwajima Project Ltd's FDA import refusal history?
Uwajima Project Ltd (FEI: 3009273035) has 3 FDA import refusal record(s) in our database, spanning from 8/27/2013 to 8/27/2013.
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. Uwajima Project Ltd's FEI number is 3009273035.
What types of violations has Uwajima Project Ltd received?
Uwajima Project 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 Uwajima Project Ltd come from?
All FDA import refusal data for Uwajima Project 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.