ACTIVATION EYEWEAR CORP
✅ Low Risk
FEI: 3009005492 • Linhai, Zhejiang • CHINA
FEI Number
3009005492
Location
Linhai, Zhejiang
Country
CHINAAddress
Yaoda Mall, Duqiao, Bldg NO F/2; 7 Yaoda Shopping, Linhai, Zhejiang, China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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
Frequently Asked Questions
What is ACTIVATION EYEWEAR CORP's FDA import refusal history?
ACTIVATION EYEWEAR CORP (FEI: 3009005492) has 1 FDA import refusal record(s) in our database, spanning from 4/11/2019 to 4/11/2019.
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. ACTIVATION EYEWEAR CORP's FEI number is 3009005492.
What types of violations has ACTIVATION EYEWEAR CORP received?
ACTIVATION EYEWEAR CORP 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 ACTIVATION EYEWEAR CORP come from?
All FDA import refusal data for ACTIVATION EYEWEAR CORP 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.