Ideal World International Ltd
⚠️ Moderate Risk
FEI: 3006497981 • Quarry Bay • HONG KONG
FEI Number
3006497981
Location
Quarry Bay
Country
HONG KONGAddress
989 King'S Road7th Floor No. 5, , Quarry Bay, , 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
Frequently Asked Questions
What is Ideal World International Ltd's FDA import refusal history?
Ideal World International Ltd (FEI: 3006497981) has 2 FDA import refusal record(s) in our database, spanning from 3/25/2009 to 3/25/2009.
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. Ideal World International Ltd's FEI number is 3006497981.
What types of violations has Ideal World International Ltd received?
Ideal World International 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 Ideal World International Ltd come from?
All FDA import refusal data for Ideal World International 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.