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Lee Hoong Kee Limited

⚠️ Moderate Risk

FEI: 3010052811 • Sheung Wan, Hong Kong Island • HONG KONG

FEI

FEI Number

3010052811

📍

Location

Sheung Wan, Hong Kong Island

🇭🇰

Country

HONG KONG
🏢

Address

17 Queen Street, , Sheung Wan, Hong Kong Island, Hong Kong

Moderate Risk

FDA Import Risk Assessment

42.6
LowModerateHighCritical

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

Statistics

12
Total Refusals
9
Unique Violations
2/10/2006
Latest Refusal
5/22/2002
Earliest Refusal

Score Breakdown

Violation Severity
67.4×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
32.2×10%
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

2497×

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.

3247×

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)).

1182×

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).

752×

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).

161×

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.

621×

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).

91×

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.

831×

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.

3211×

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

DateProductViolationsDivision
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/10/2006
17YGT99MEAT AND MEAT PRODUCTS N.E.C., MEAT/EXOTIC MEAT PRODUCTS, N.E.C.
249FILTHY
324NO ENGLISH
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.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
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
321LACKS N/C
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/22/2002
54GBH99ANIMAL BY-PRODUCTS AND EXTRACTS, N.E.C.
249FILTHY
9SALMONELLA
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.