Aoma Intl. Co Ltd
⚠️ High Risk
FEI: 3010875039 • Shenzhen • CHINA
FEI Number
3010875039
Location
Shenzhen
Country
CHINAAddress
2201 Cai Tian Road, , 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
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).
RX DEVICE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.
Refusal History
Frequently Asked Questions
What is Aoma Intl. Co Ltd's FDA import refusal history?
Aoma Intl. Co Ltd (FEI: 3010875039) has 1 FDA import refusal record(s) in our database, spanning from 9/10/2024 to 9/10/2024.
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. Aoma Intl. Co Ltd's FEI number is 3010875039.
What types of violations has Aoma Intl. Co Ltd received?
Aoma Intl. 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 Aoma Intl. Co Ltd come from?
All FDA import refusal data for Aoma Intl. 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.