Golden Resources Development Ltd.
⚠️ Moderate Risk
FEI: 3013259049 • Tsing Yi, New Territories • HONG KONG
FEI Number
3013259049
Location
Tsing Yi, New Territories
Country
HONG KONGAddress
11/F, Golden Resources Centre; 2-12 Cheung Tat Road; Island, Tsing Yi, New Territories, 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.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
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).
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.
UNSFDIETLB
The article appears to be a dietary supplement or contain a dietary ingredient that presents a significant or unreasonable risk of illness or injury under the conditions of use set out in the labeling or, if none are set out in the labeling, under customary conditions of use.
SACCHARLBL
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
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).
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).
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.
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).
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/16/2016 | 02DGT09RICE, JASMINE, PROCESSED (PACKAGED) | 241PESTICIDE | Los Angeles District Office (LOS-DO) |
| 12/16/2016 | 02DGT09RICE, JASMINE, PROCESSED (PACKAGED) | 241PESTICIDE | Los Angeles District Office (LOS-DO) |
| 8/6/2003 | 25PGH03MUSHROOM, STRAW, WHOLE (BUTTON) (FUNGI) | 157FOREIGN OB | New York District Office (NYK-DO) |
| 4/22/2003 | 22BGH04WATERMELON, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 4/22/2003 | 33SGT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE) | 11UNSAFE COL | New York District Office (NYK-DO) |
| 3/5/2002 | 25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 3/5/2002 | 25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 3/5/2002 | 25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 3/5/2002 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | New York District Office (NYK-DO) | |
| 2/24/2002 | 25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 2/24/2002 | 25SGH09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 2/8/2002 | 54EGT99HERBALS & BOTANICAL TEAS, N.E.C. | 2460UNSFDIETLB | New York District Office (NYK-DO) |
| 2/8/2002 | 54EGT99HERBALS & BOTANICAL TEAS, N.E.C. | New York District Office (NYK-DO) | |
| 10/9/2001 | 25SGH99FUNGI PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Golden Resources Development Ltd.'s FDA import refusal history?
Golden Resources Development Ltd. (FEI: 3013259049) has 14 FDA import refusal record(s) in our database, spanning from 10/9/2001 to 12/16/2016.
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 Resources Development Ltd.'s FEI number is 3013259049.
What types of violations has Golden Resources Development Ltd. received?
Golden Resources Development Ltd. has been cited for 11 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 Resources Development Ltd. come from?
All FDA import refusal data for Golden Resources Development 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.