Goldensign International Technology Co.Ltd
✅ Low Risk
FEI: 3009522273 • Shanghai, Shanghai • CHINA
FEI Number
3009522273
Location
Shanghai, Shanghai
Country
CHINAAddress
Room 2212-2216 Floor 22nd, No. 58 Jinxin Road; Jinqiaozhen Pudongxin, Shanghai, Shanghai, China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
NO TAG
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
Refusal History
Frequently Asked Questions
What is Goldensign International Technology Co.Ltd's FDA import refusal history?
Goldensign International Technology Co.Ltd (FEI: 3009522273) has 1 FDA import refusal record(s) in our database, spanning from 9/6/2019 to 9/6/2019.
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. Goldensign International Technology Co.Ltd's FEI number is 3009522273.
What types of violations has Goldensign International Technology Co.Ltd received?
Goldensign International Technology Co.Ltd has been cited for 2 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 Goldensign International Technology Co.Ltd come from?
All FDA import refusal data for Goldensign International Technology Co.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.