ANAREN INDUSTRIAL LIMITED
⚠️ Moderate Risk
FEI: 3025095679 • Tsim Sha Tsui, Kowloon • HONG KONG
FEI Number
3025095679
Location
Tsim Sha Tsui, Kowloon
Country
HONG KONGAddress
9/F, Glory Centre; 8 Hillwood Road, Tsim Sha Tsui, Kowloon, 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).
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.
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 ANAREN INDUSTRIAL LIMITED's FDA import refusal history?
ANAREN INDUSTRIAL LIMITED (FEI: 3025095679) has 2 FDA import refusal record(s) in our database, spanning from 5/1/2023 to 2/21/2025.
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. ANAREN INDUSTRIAL LIMITED's FEI number is 3025095679.
What types of violations has ANAREN INDUSTRIAL LIMITED received?
ANAREN INDUSTRIAL LIMITED 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 ANAREN INDUSTRIAL LIMITED come from?
All FDA import refusal data for ANAREN INDUSTRIAL 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.