SHENZHEN UMIGHTY VAPE TECH CO.,LTD
⚠️ Moderate Risk
FEI: 3023522859 • Guandong • CHINA
FEI Number
3023522859
Location
Guandong
Country
CHINAAddress
Baoan Dist, 4/F, Xinlong Technologypark; Dawangshan Industrial Road Shajing Town, Guandong, , 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
TP FLAVOR
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/25/2022 | 98MCA01E-LIQUID | 3520TP FLAVOR | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is SHENZHEN UMIGHTY VAPE TECH CO.,LTD's FDA import refusal history?
SHENZHEN UMIGHTY VAPE TECH CO.,LTD (FEI: 3023522859) has 1 FDA import refusal record(s) in our database, spanning from 8/25/2022 to 8/25/2022.
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. SHENZHEN UMIGHTY VAPE TECH CO.,LTD's FEI number is 3023522859.
What types of violations has SHENZHEN UMIGHTY VAPE TECH CO.,LTD received?
SHENZHEN UMIGHTY VAPE TECH CO.,LTD has been cited for 1 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 SHENZHEN UMIGHTY VAPE TECH CO.,LTD come from?
All FDA import refusal data for SHENZHEN UMIGHTY VAPE TECH 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.