Abbott Vascular Devices Holland B.V.
⚠️ Moderate Risk
FEI: 3004091615 • Ulestraten, Limburg • NETHERLANDS
FEI Number
3004091615
Location
Ulestraten, Limburg
Country
NETHERLANDSAddress
Bamfordweg 1, , Ulestraten, Limburg, Netherlands
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).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
Refusal History
Frequently Asked Questions
What is Abbott Vascular Devices Holland B.V.'s FDA import refusal history?
Abbott Vascular Devices Holland B.V. (FEI: 3004091615) has 1 FDA import refusal record(s) in our database, spanning from 12/16/2011 to 12/16/2011.
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. Abbott Vascular Devices Holland B.V.'s FEI number is 3004091615.
What types of violations has Abbott Vascular Devices Holland B.V. received?
Abbott Vascular Devices Holland B.V. 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 Abbott Vascular Devices Holland B.V. come from?
All FDA import refusal data for Abbott Vascular Devices Holland B.V. 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.