ALD GROUP LIMITED
⚠️ High Risk
FEI: 3012424080 • Shenzhen • CHINA
FEI Number
3012424080
Location
Shenzhen
Country
CHINAAddress
Ald Building No.2 Indus, Community, Shenzhen, , China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
TP NO PMTA
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 FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.
TP NO SE
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 FDA has found to be misbranded under section 903(a)(6) of the FD&C Act in that a notice or other information respecting it was not provided as required by section 905(j).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/1/2025 | 98LEA02E-CIGARETTE, KIT | Division of West Coast Imports (DWCI) | |
| 12/1/2025 | 98LEA02E-CIGARETTE, KIT | Division of West Coast Imports (DWCI) | |
| 12/1/2025 | 98LEA02E-CIGARETTE, KIT | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is ALD GROUP LIMITED's FDA import refusal history?
ALD GROUP LIMITED (FEI: 3012424080) has 3 FDA import refusal record(s) in our database, spanning from 12/1/2025 to 12/1/2025.
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. ALD GROUP LIMITED's FEI number is 3012424080.
What types of violations has ALD GROUP LIMITED received?
ALD GROUP LIMITED 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 ALD GROUP LIMITED come from?
All FDA import refusal data for ALD GROUP 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.