Lee Hoong Kee Limited
⚠️ Moderate Risk
FEI: 3010052811 • Sheung Wan, Hong Kong Island • HONG KONG
FEI Number
3010052811
Location
Sheung Wan, Hong Kong Island
Country
HONG KONGAddress
17 Queen Street, , Sheung Wan, Hong Kong Island, Hong Kong
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.
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)).
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).
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
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).
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.
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.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/10/2006 | 17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 10/4/2005 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 10/4/2005 | 60LBJ99ANALGESIC, N.E.C. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
| 9/12/2005 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | Los Angeles District Office (LOS-DO) | |
| 2/9/2005 | 54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 324NO ENGLISH | Los Angeles District Office (LOS-DO) |
| 5/5/2003 | 21VEE07PINEAPPLE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 5/22/2002 | 54GBH99ANIMAL BY-PRODUCTS AND EXTRACTS, N.E.C. | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Lee Hoong Kee Limited's FDA import refusal history?
Lee Hoong Kee Limited (FEI: 3010052811) has 12 FDA import refusal record(s) in our database, spanning from 5/22/2002 to 2/10/2006.
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. Lee Hoong Kee Limited's FEI number is 3010052811.
What types of violations has Lee Hoong Kee Limited received?
Lee Hoong Kee Limited has been cited for 9 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 Lee Hoong Kee Limited come from?
All FDA import refusal data for Lee Hoong Kee 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.