APPARE SUISAN HIMEJI BRANCH
⚠️ Moderate Risk
FEI: 3010233781 • Himeji, Hyogo • JAPAN
FEI Number
3010233781
Location
Himeji, Hyogo
Country
JAPANAddress
912-18, Shirahama-Cho, Himeji, Hyogo, 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/19/2017 | 16AGN01ANCHOVY | 249FILTHY | Division of West Coast Imports (DWCI) |
| 9/19/2017 | 16AGN01ANCHOVY | 249FILTHY | Division of West Coast Imports (DWCI) |
| 7/12/2017 | 16AGN01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
| 7/12/2017 | 16AGN01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is APPARE SUISAN HIMEJI BRANCH's FDA import refusal history?
APPARE SUISAN HIMEJI BRANCH (FEI: 3010233781) has 4 FDA import refusal record(s) in our database, spanning from 7/12/2017 to 9/19/2017.
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. APPARE SUISAN HIMEJI BRANCH's FEI number is 3010233781.
What types of violations has APPARE SUISAN HIMEJI BRANCH received?
APPARE SUISAN HIMEJI BRANCH 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 APPARE SUISAN HIMEJI BRANCH come from?
All FDA import refusal data for APPARE SUISAN HIMEJI BRANCH 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.