TANIGUCHI KAISAN CO.,LTD.
⚠️ Moderate Risk
FEI: 3008380993 • Shibushi, Kagoshima • JAPAN
FEI Number
3008380993
Location
Shibushi, Kagoshima
Country
JAPANAddress
584-1, Shibushicho-Cho, Shibushi, Kagoshima, 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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/22/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 9/22/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 9/22/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 9/22/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 1/28/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 1/28/2016 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 6/28/2011 | 16AGT01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is TANIGUCHI KAISAN CO.,LTD.'s FDA import refusal history?
TANIGUCHI KAISAN CO.,LTD. (FEI: 3008380993) has 7 FDA import refusal record(s) in our database, spanning from 6/28/2011 to 9/22/2016.
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. TANIGUCHI KAISAN CO.,LTD.'s FEI number is 3008380993.
What types of violations has TANIGUCHI KAISAN CO.,LTD. received?
TANIGUCHI KAISAN 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 TANIGUCHI KAISAN CO.,LTD. come from?
All FDA import refusal data for TANIGUCHI KAISAN 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.