Everife Intl Ltd
⚠️ Moderate Risk
FEI: 3004009133 • Kwun Tong • HONG KONG
FEI Number
3004009133
Location
Kwun Tong
Country
HONG KONGAddress
19 24 Shing Yip St, , Kwun Tong, , 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).
NOT IMPACT
The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/7/2003 | 86HQZFRAME, SPECTACLE | Cincinnati District Office (CIN-DO) | |
| 8/7/2003 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | Cincinnati District Office (CIN-DO) | |
| 8/7/2003 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Everife Intl Ltd's FDA import refusal history?
Everife Intl Ltd (FEI: 3004009133) has 3 FDA import refusal record(s) in our database, spanning from 8/7/2003 to 8/7/2003.
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. Everife Intl Ltd's FEI number is 3004009133.
What types of violations has Everife Intl Ltd received?
Everife Intl Ltd has been cited for 3 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 Everife Intl Ltd come from?
All FDA import refusal data for Everife Intl 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.