True World Japan
⚠️ Moderate Risk
FEI: 3005255865 • Tokyo • 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
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
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 |
|---|---|---|---|
| 6/29/2011 | 16AGH33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | San Francisco District Office (SAN-DO) | |
| 5/17/2011 | 25JGI14TURNIP (ROOT & TUBER VEGETABLE) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 24TGT29SEAWEED (LEAF & STEM VEGETABLE) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 27BGT99NON-STANDARDIZED DRESSING, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 27VGT02DISTILLED VINEGAR [ MALT, GLUCOSE (DEXTROSE) AND SUGAR (SUCROSE)] | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 37JGT05SOY SAUCE | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 25YGP99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 5/17/2011 | 16YGT99FISHERY PRODUCTS, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 1/4/2011 | 25JGN18LOTUS ROOT (ROOT & TUBER VEGETABLE) | New York District Office (NYK-DO) | |
| 3/18/2009 | 03FGT07RICE CRACKERS | 324NO ENGLISH | San Francisco District Office (SAN-DO) |
| 3/18/2009 | 03FGT07RICE CRACKERS | 324NO ENGLISH | San Francisco District Office (SAN-DO) |
| 6/8/2006 | 16YGH08SHARK FIN, FISHERY PRODUCTS, N.E.C. | 249FILTHY | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is True World Japan's FDA import refusal history?
True World Japan (FEI: 3005255865) has 12 FDA import refusal record(s) in our database, spanning from 6/8/2006 to 6/29/2011.
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. True World Japan's FEI number is 3005255865.
What types of violations has True World Japan received?
True World Japan has been cited for 6 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 True World Japan come from?
All FDA import refusal data for True World Japan 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.