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Golden Gate Supply Limited

⚠️ Moderate Risk

FEI: 3010130162 • 'None', Not Applicable • HONG KONG

FEI

FEI Number

3010130162

📍

Location

'None', Not Applicable

🇭🇰

Country

HONG KONG
🏢

Address

40 Man Cheong Bldg.,G/F., Ferry Point, Kowloon., 'None', Not Applicable, Hong Kong

Moderate Risk

FDA Import Risk Assessment

38.2
LowModerateHighCritical

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

Statistics

7
Total Refusals
13
Unique Violations
8/1/2012
Latest Refusal
9/17/2008
Earliest Refusal

Score Breakdown

Violation Severity
65.8×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
18.1×10%
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

2494×

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.

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.

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

27201×

DULCIN

The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409

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.

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.

3241×

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)).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4871×

SACCHARIN

The article contains Saccharin, a non-nutritive sweetner, and its label or labeling fails to bear the required warning statement.

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).

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.

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.

26401×

CYCLAMATE

The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409

Refusal History

DateProductViolationsDivision
8/1/2012
29BET60SODA WATER, CARBONATED
218LIST INGRE
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
1/24/2012
24TCT12CHINESE CABBAGE, CELERY CABBAGE (LEAF & STEM VEGETABLE)
320LACKS FIRM
324NO ENGLISH
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/7/2011
33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
11/2/2010
21IFT16CHINESE RED DATES (JUJUBES, ZIZIPHUS, JUJUBA (PIT FRUIT PUREES)
249FILTHY
New York District Office (NYK-DO)
10/5/2010
21IFT16CHINESE RED DATES (JUJUBES, ZIZIPHUS, JUJUBA (PIT FRUIT PUREES)
249FILTHY
New York District Office (NYK-DO)
10/5/2010
21IFT16CHINESE RED DATES (JUJUBES, ZIZIPHUS, JUJUBA (PIT FRUIT PUREES)
249FILTHY
New York District Office (NYK-DO)
9/17/2008
21GGT09OLIVES (PIT FRUIT)
11UNSAFE COL
249FILTHY
2640CYCLAMATE
2720DULCIN
487SACCHARIN
New York District Office (NYK-DO)

Frequently Asked Questions

What is Golden Gate Supply Limited's FDA import refusal history?

Golden Gate Supply Limited (FEI: 3010130162) has 7 FDA import refusal record(s) in our database, spanning from 9/17/2008 to 8/1/2012.

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. Golden Gate Supply Limited's FEI number is 3010130162.

What types of violations has Golden Gate Supply Limited received?

Golden Gate Supply Limited has been cited for 13 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 Golden Gate Supply Limited come from?

All FDA import refusal data for Golden Gate Supply 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.