KWONG HUNG SENG LTD.
⚠️ Moderate Risk
FEI: 3004354339 • Sam Pran, Nakorn Pathom • THAILAND
FEI Number
3004354339
Location
Sam Pran, Nakorn Pathom
Country
THAILANDAddress
5, Kratumlom, Sam Pran, Sam Pran, Nakorn Pathom, Thailand
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/12/2012 | 37JCP15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 11/22/2011 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 9/27/2011 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | Seattle District Office (SEA-DO) |
| 8/11/2011 | 37JCP15BEAN, YELLOW SAUCE | 249FILTHY | Chicago District Office (CHI-DO) |
| 7/6/2010 | 37JCE99SAUCES, N.E.C. | San Francisco District Office (SAN-DO) | |
| 6/21/2010 | 37KCT15BEAN, YELLOW PASTE | 249FILTHY | Seattle District Office (SEA-DO) |
| 4/24/2008 | 37JCT05SOY SAUCE | 83NO PROCESS | New York District Office (NYK-DO) |
| 1/12/2007 | 24BGH13SOYBEANS (SEE INDUSTRY 37 FOR BEAN CURD), DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 8/21/2006 | 24ACT99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE) | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 1/18/2006 | 63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 1/18/2006 | 63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 8/11/2005 | 37JCP15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 3/8/2005 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | New York District Office (NYK-DO) |
| 2/1/2005 | 37JCP15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 8/21/2003 | 37JCP15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 6/17/2003 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/17/2002 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 1/24/2002 | 37JCT15BEAN, YELLOW SAUCE | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is KWONG HUNG SENG LTD.'s FDA import refusal history?
KWONG HUNG SENG LTD. (FEI: 3004354339) has 18 FDA import refusal record(s) in our database, spanning from 1/24/2002 to 10/12/2012.
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. KWONG HUNG SENG LTD.'s FEI number is 3004354339.
What types of violations has KWONG HUNG SENG LTD. received?
KWONG HUNG SENG LTD. 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 KWONG HUNG SENG LTD. come from?
All FDA import refusal data for KWONG HUNG SENG 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.