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Master Kong Holdings Limited

⚠️ Moderate Risk

FEI: 3009479482 • Tianjin, Tianjin • CHINA

FEI

FEI Number

3009479482

📍

Location

Tianjin, Tianjin

🇨🇳

Country

CHINA
🏢

Address

3rd Street,Tianjin, , Tianjin, Tianjin, China

Moderate Risk

FDA Import Risk Assessment

43.2
LowModerateHighCritical

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

Statistics

12
Total Refusals
9
Unique Violations
11/27/2013
Latest Refusal
6/11/2013
Earliest Refusal

Score Breakdown

Violation Severity
52.2×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
100.0×10%
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

32412×

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)).

837×

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.

626×

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).

3214×

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.

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

2382×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

3201×

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.

2181×

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.

Refusal History

DateProductViolationsDivision
11/27/2013
31KGE02TEA, GREEN
324NO ENGLISH
New York District Office (NYK-DO)
11/27/2013
31KGE20TEA, LIQUID
324NO ENGLISH
New York District Office (NYK-DO)
11/27/2013
31KGE02TEA, GREEN
324NO ENGLISH
New York District Office (NYK-DO)
11/27/2013
31KGE20TEA, LIQUID
324NO ENGLISH
New York District Office (NYK-DO)
11/26/2013
31KGE02TEA, GREEN
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
11/26/2013
31KGE20TEA, LIQUID
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
11/26/2013
31KGE02TEA, GREEN
321LACKS N/C
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
9/18/2013
31KHE99TEA, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
9/18/2013
31KHE99TEA, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
9/4/2013
31KGE99TEA, N.E.C.
324NO ENGLISH
83NO PROCESS
Division of Northeast Imports (DNEI)
6/11/2013
31KGT02TEA, GREEN
238UNSAFE ADD
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/11/2013
31KGT01TEA, BLACK
238UNSAFE ADD
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Master Kong Holdings Limited's FDA import refusal history?

Master Kong Holdings Limited (FEI: 3009479482) has 12 FDA import refusal record(s) in our database, spanning from 6/11/2013 to 11/27/2013.

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. Master Kong Holdings Limited's FEI number is 3009479482.

What types of violations has Master Kong Holdings Limited received?

Master Kong Holdings 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 Master Kong Holdings Limited come from?

All FDA import refusal data for Master Kong Holdings 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.