K K TECHNOLOGY CO. LTD
⚠️ Moderate Risk
FEI: 3016610846 • Shenzhen • CHINA
FEI Number
3016610846
Location
Shenzhen
Country
CHINAAddress
4fl, Bldg A3, Fuyuan Industrial Zone. 600,Fengtang Ave,Tangwei Community,Fuyong St, Baoan Dist, , Shenzhen, , China
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
TPLACKFIRM
This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.
TPLKUSSLLB
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.
TPLACKSNC
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(B) of the FD&C Act in that the label does not provide an accurate statement of the quantity of contents in terms of weight, measure or numerical count.
TPNICWARN
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that appears to be misbranded under section 903(a)(7)(B) in that it is sold or distributed in violation of regulations prescribed under 906(d), namely its package fails to bear the required warning statement "WARNING: This product contains nicotine. Nicotine is an addictive chemical." Or if applicable the required statement "This product is made from tobacco."
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/17/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 7/17/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 7/17/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 7/17/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 7/17/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 7/15/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of West Coast Imports (DWCI) | |
| 6/30/2020 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is K K TECHNOLOGY CO. LTD's FDA import refusal history?
K K TECHNOLOGY CO. LTD (FEI: 3016610846) has 7 FDA import refusal record(s) in our database, spanning from 6/30/2020 to 7/17/2020.
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. K K TECHNOLOGY CO. LTD's FEI number is 3016610846.
What types of violations has K K TECHNOLOGY CO. LTD received?
K K TECHNOLOGY CO. LTD has been cited for 4 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 K K TECHNOLOGY CO. LTD come from?
All FDA import refusal data for K K 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.