Polymax Development Co Ltd
⚠️ Moderate Risk
FEI: 3002867018 • Causeway Bay • HONG KONG
FEI Number
3002867018
Location
Causeway Bay
Country
HONG KONGAddress
463-483 Lockhart Rd, , Causeway 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
Frequently Asked Questions
What is Polymax Development Co Ltd's FDA import refusal history?
Polymax Development Co Ltd (FEI: 3002867018) has 2 FDA import refusal record(s) in our database, spanning from 12/25/2003 to 1/16/2004.
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. Polymax Development Co Ltd's FEI number is 3002867018.
What types of violations has Polymax Development Co Ltd received?
Polymax Development Co 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 Polymax Development Co Ltd come from?
All FDA import refusal data for Polymax Development Co 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.