First Lotus Worldwide Limited
⚠️ Moderate Risk
FEI: 3008281123 • Hong Kong • HONG KONG
FEI Number
3008281123
Location
Hong Kong
Country
HONG KONGAddress
Flat/Rm 602h 6/F Lai Cheung Factory, , Hong Kong, , Hong Kong
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
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).
Refusal History
Frequently Asked Questions
What is First Lotus Worldwide Limited's FDA import refusal history?
First Lotus Worldwide Limited (FEI: 3008281123) has 2 FDA import refusal record(s) in our database, spanning from 6/17/2010 to 6/17/2010.
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. First Lotus Worldwide Limited's FEI number is 3008281123.
What types of violations has First Lotus Worldwide Limited received?
First Lotus Worldwide Limited 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 First Lotus Worldwide Limited come from?
All FDA import refusal data for First Lotus Worldwide 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.