HANGHAI MEDICAL PRODUCTS CO LTD
⚠️ Moderate Risk
FEI: 3012664467 • Yongkang • CHINA
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
POSS N/STR
The article appears to consist in whole or in part of any filthy, putrid, or decomposed substance, namely, potentially infectious organisms
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/20/2018 | 80FQMBANDAGE, ELASTIC | 2800POSS N/STR | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is HANGHAI MEDICAL PRODUCTS CO LTD's FDA import refusal history?
HANGHAI MEDICAL PRODUCTS CO LTD (FEI: 3012664467) has 1 FDA import refusal record(s) in our database, spanning from 4/20/2018 to 4/20/2018.
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. HANGHAI MEDICAL PRODUCTS CO LTD's FEI number is 3012664467.
What types of violations has HANGHAI MEDICAL PRODUCTS CO LTD received?
HANGHAI MEDICAL PRODUCTS 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 HANGHAI MEDICAL PRODUCTS CO LTD come from?
All FDA import refusal data for HANGHAI MEDICAL PRODUCTS 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.