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Sinojet Development Ltd

⚠️ Moderate Risk

FEI: 3003894225 • Guang Dong • CHINA

FEI

FEI Number

3003894225

📍

Location

Guang Dong

🇨🇳

Country

CHINA
🏢

Address

#75 2f/L Dong Phong Road Hou Streetdong, , Guang Dong, , China

Moderate Risk

FDA Import Risk Assessment

47.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

14
Total Refusals
12
Unique Violations
12/14/2011
Latest Refusal
11/9/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.8×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
19.7×10%
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

24910×

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.

113×

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).

3242×

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)).

2511×

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:

26401×

CYCLAMATE

The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409

26801×

SACCHARLBL

The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient

27201×

DULCIN

The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409

34211×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4821×

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.

20401×

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.

2181×

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

DateProductViolationsDivision
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.
251POISONOUS
3421MELAMINE
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.
2040SULFITELBL
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
3/24/2010
24TGT27TURNIP GREENS (LEAF & STEM VEGETABLE)
218LIST INGRE
249FILTHY
New York District Office (NYK-DO)
2/3/2010
21TGT03FIG, DRIED OR PASTE
11UNSAFE COL
249FILTHY
2640CYCLAMATE
2680SACCHARLBL
2720DULCIN
New York District Office (NYK-DO)
7/2/2009
24TGH99LEAF & STEM VEGETABLES, N.E.C.
249FILTHY
324NO ENGLISH
New York District Office (NYK-DO)
7/2/2009
24TGH99LEAF & STEM VEGETABLES, N.E.C.
249FILTHY
324NO ENGLISH
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.