Sinojet Development Ltd
⚠️ Moderate Risk
FEI: 3003894225 • Guang Dong • CHINA
FEI Number
3003894225
Location
Guang Dong
Country
CHINAAddress
#75 2f/L Dong Phong Road Hou Streetdong, , Guang Dong, , China
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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)).
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
SACCHARLBL
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
DULCIN
The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409
MELAMINE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to bear or contain a food additive, namely melamine and/or a melamine analog, that is unsafe within the meaning of section 409.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/14/2011 | 25PGH10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 249FILTHY | New York District Office (NYK-DO) |
| 12/14/2011 | 25PGT10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 249FILTHY | New York District Office (NYK-DO) |
| 12/14/2011 | 25PGH10FUNGUS, WHITE, WHOLE (BUTTON) (FUNGI) | 249FILTHY | New York District Office (NYK-DO) |
| 7/13/2011 | 03AGT99BREAD/ROLLS/BUNS, N.E.C. | New York District Office (NYK-DO) | |
| 2/22/2011 | 54FBT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 3/24/2010 | 25FGH99MIXED VEGETABLES, DRIED OR PASTE, N.E.C. | New York District Office (NYK-DO) | |
| 3/24/2010 | 24TGT27TURNIP GREENS (LEAF & STEM VEGETABLE) | New York District Office (NYK-DO) | |
| 2/3/2010 | 21TGT03FIG, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 7/2/2009 | 24TGH99LEAF & STEM VEGETABLES, N.E.C. | New York District Office (NYK-DO) | |
| 7/2/2009 | 24TGH99LEAF & STEM VEGETABLES, N.E.C. | New York District Office (NYK-DO) | |
| 6/28/2006 | 37BCT27BEAN CURD, FRESH - SOFT OR HARD (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS) | 249FILTHY | New York District Office (NYK-DO) |
| 10/11/2005 | 24HGT08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 11/9/2004 | 23KGT05MELON SEEDS (EDIBLE SEED) | 11UNSAFE COL | New York District Office (NYK-DO) |
| 11/9/2004 | 23KGT05MELON SEEDS (EDIBLE SEED) | 11UNSAFE COL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Sinojet Development Ltd's FDA import refusal history?
Sinojet Development Ltd (FEI: 3003894225) has 14 FDA import refusal record(s) in our database, spanning from 11/9/2004 to 12/14/2011.
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. Sinojet Development Ltd's FEI number is 3003894225.
What types of violations has Sinojet Development Ltd received?
Sinojet Development Ltd has been cited for 12 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 Sinojet Development Ltd come from?
All FDA import refusal data for Sinojet Development 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.