Inaba Shokuhin Kk
⚠️ Moderate Risk
FEI: 3003415938 • Ihara-gun, Shizuoka-ken • JAPAN
FEI Number
3003415938
Location
Ihara-gun, Shizuoka-ken
Country
JAPANAddress
114-1, Kitada, Yuicho, , Ihara-gun, Shizuoka-ken, 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
REFUSE EI
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.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/14/2017 | 16AET07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 2/14/2017 | 16AET07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 10/31/2012 | 16AGT07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 3/28/2012 | 16AEN07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 3/5/2012 | 16AEN07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 3/5/2012 | 16AEN07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 3/5/2012 | 16AEN07BONITO | 3600REFUSE EI | Los Angeles District Office (LOS-DO) |
| 12/16/2011 | 23KGN03SOYBEANS (EDIBLE SEED) | 3600REFUSE EI | New York District Office (NYK-DO) |
| 9/16/2005 | 24AGT07KIDNEY BEAN | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Inaba Shokuhin Kk's FDA import refusal history?
Inaba Shokuhin Kk (FEI: 3003415938) has 9 FDA import refusal record(s) in our database, spanning from 9/16/2005 to 2/14/2017.
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. Inaba Shokuhin Kk's FEI number is 3003415938.
What types of violations has Inaba Shokuhin Kk received?
Inaba Shokuhin Kk has been cited for 4 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 Inaba Shokuhin Kk come from?
All FDA import refusal data for Inaba Shokuhin Kk 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.