Q.P.Co.,Ltd
⚠️ High Risk
FEI: 2000005687 • Shibuya, Tokyo • JAPAN
FEI Number
2000005687
Location
Shibuya, Tokyo
Country
JAPANAddress
1 Chome 4-13 None, Shibuya, Shibuya, Tokyo, Japan
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 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.
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)).
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).
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/23/2003 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 10/25/2002 | 16YGN04FISH ROE, FISHERY PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 9/12/2002 | 37JHT99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 9/11/2002 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | Los Angeles District Office (LOS-DO) | |
| 9/11/2002 | 02DGT99RICE, PROCESSED (PACKAGED) N.E.C. | Los Angeles District Office (LOS-DO) | |
| 9/11/2002 | 16YGN04FISH ROE, FISHERY PRODUCTS, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 9/11/2002 | 37JGE99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 9/11/2002 | 37JGE99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 9/4/2002 | 37JGT99SAUCES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 5/10/2002 | 38YEE99SOUP, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 5/10/2002 | 37JEE99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 5/6/2002 | 37JHT08TOMATO SAUCE (WITH OTHER INGREDIENTS) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Q.P.Co.,Ltd's FDA import refusal history?
Q.P.Co.,Ltd (FEI: 2000005687) has 12 FDA import refusal record(s) in our database, spanning from 5/6/2002 to 4/23/2003.
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. Q.P.Co.,Ltd's FEI number is 2000005687.
What types of violations has Q.P.Co.,Ltd received?
Q.P.Co.,Ltd has been cited for 5 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 Q.P.Co.,Ltd come from?
All FDA import refusal data for Q.P.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.