Morii Shokuhin Co Ltd
⚠️ Moderate Risk
FEI: 1000267672 • Sakurai • 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
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 |
|---|---|---|---|
| 2/25/2015 | 25PGT04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI) | 62NEEDS FCE | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Morii Shokuhin Co Ltd's FDA import refusal history?
Morii Shokuhin Co Ltd (FEI: 1000267672) has 1 FDA import refusal record(s) in our database, spanning from 2/25/2015 to 2/25/2015.
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. Morii Shokuhin Co Ltd's FEI number is 1000267672.
What types of violations has Morii Shokuhin Co Ltd received?
Morii Shokuhin 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 Morii Shokuhin Co Ltd come from?
All FDA import refusal data for Morii Shokuhin 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.