AngioDynamics, Inc.
⚠️ Moderate Risk
FEI: 3017892510 • Glens Falls, NY • UNITED STATES
FEI Number
3017892510
Location
Glens Falls, NY
Country
UNITED STATESAddress
8 Glens Falls Tech Park, , Glens Falls, NY, United States
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
DV QUALITY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/5/2009 | 74DQXWIRE, GUIDE, CATHETER | New York District Office (NYK-DO) | |
| 5/5/2009 | 78MSDCATHETER, HEMODIALYSIS, IMPLANTED | 479DV QUALITY | New York District Office (NYK-DO) |
| 5/5/2009 | 78MSDCATHETER, HEMODIALYSIS, IMPLANTED | 479DV QUALITY | New York District Office (NYK-DO) |
| 5/5/2009 | 74DQXWIRE, GUIDE, CATHETER | New York District Office (NYK-DO) | |
| 5/5/2009 | 74DQXWIRE, GUIDE, CATHETER | New York District Office (NYK-DO) | |
| 5/5/2009 | 74DQXWIRE, GUIDE, CATHETER | New York District Office (NYK-DO) |
Frequently Asked Questions
What is AngioDynamics, Inc.'s FDA import refusal history?
AngioDynamics, Inc. (FEI: 3017892510) has 6 FDA import refusal record(s) in our database, spanning from 5/5/2009 to 5/5/2009.
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. AngioDynamics, Inc.'s FEI number is 3017892510.
What types of violations has AngioDynamics, Inc. received?
AngioDynamics, Inc. 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 AngioDynamics, Inc. come from?
All FDA import refusal data for AngioDynamics, Inc. 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.