Shengfeng Limited Company
⚠️ High Risk
FEI: 3007055224 • Zhongshan, Guangdong • CHINA
FEI Number
3007055224
Location
Zhongshan, Guangdong
Country
CHINAAddress
No. 88 Caihong Road, Xuzhen Shenwanzhen, Zhongshan, Guangdong, China
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
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:
UNFIT4FOOD
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.
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.
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.
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.
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).
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/15/2009 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 12/15/2009 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 11/20/2009 | 03HGT06FRUIT FILLED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/20/2009 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 11/20/2009 | 03RGT02CAKES, FILLED (OTHER THAN FRUIT OR JELLY) | 64YELLOW #5 | Los Angeles District Office (LOS-DO) |
| 11/20/2009 | 03RGT02CAKES, FILLED (OTHER THAN FRUIT OR JELLY) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
| 10/19/2009 | 23BGT15GINKGO, GINGKO NUT, SHELLED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Shengfeng Limited Company's FDA import refusal history?
Shengfeng Limited Company (FEI: 3007055224) has 7 FDA import refusal record(s) in our database, spanning from 10/19/2009 to 12/15/2009.
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. Shengfeng Limited Company's FEI number is 3007055224.
What types of violations has Shengfeng Limited Company received?
Shengfeng Limited Company has been cited for 8 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 Shengfeng Limited Company come from?
All FDA import refusal data for Shengfeng Limited Company 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.