Silklon Limited
⚠️ Moderate Risk
FEI: 3004337010 • Jiangmen City, Yandong • CHINA
FEI Number
3004337010
Location
Jiangmen City, Yandong
Country
CHINAAddress
No. 3 Liwan Developing, Xinhui District, Jiangmen City, Yandong, 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.
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.
INCONSPICU
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)).
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/6/2012 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | San Francisco District Office (SAN-DO) |
| 6/21/2011 | 25LGT15WATER CHESTNUT, DRIED OR PASTE | San Francisco District Office (SAN-DO) | |
| 6/21/2011 | 23BGT05COCONUT, SHELLED | San Francisco District Office (SAN-DO) | |
| 10/23/2009 | 21HGH16CHINESE RED DATE (JUJUBES, ZIZIPHUS JUJUBA), DRIED OR PASTE | 249FILTHY | San Francisco District Office (SAN-DO) |
| 1/11/2008 | 16YGH07FISH MAW, FISHERY PRODUCTS, N.E.C. | 249FILTHY | San Francisco District Office (SAN-DO) |
| 12/28/2007 | 16YGH07FISH MAW, FISHERY PRODUCTS, N.E.C. | 249FILTHY | San Francisco District Office (SAN-DO) |
| 8/8/2005 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Silklon Limited's FDA import refusal history?
Silklon Limited (FEI: 3004337010) has 7 FDA import refusal record(s) in our database, spanning from 8/8/2005 to 7/6/2012.
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. Silklon Limited's FEI number is 3004337010.
What types of violations has Silklon Limited received?
Silklon Limited has been cited for 4 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 Silklon Limited come from?
All FDA import refusal data for Silklon Limited 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.