CareFusion DR 203 LTD
⚠️ Moderate Risk
FEI: 3007019930 • Santo Domingo, Distrito Nacional • DOMINICAN REPUBLIC
FEI Number
3007019930
Location
Santo Domingo, Distrito Nacional
Country
DOMINICAN REPUBLICAddress
Americas Km22, Edif 1-2, Zona Franca Las Americas, Km 22 E-1, Santo Domingo, Distrito Nacional, Dominican Republic
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
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/26/2011 | 78FSHTRAY, SURGICAL, NEEDLE | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 7/26/2011 | 78KNWINSTRUMENT, BIOPSY | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 7/26/2011 | 78KNWINSTRUMENT, BIOPSY | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 7/26/2011 | 78KNWINSTRUMENT, BIOPSY | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is CareFusion DR 203 LTD's FDA import refusal history?
CareFusion DR 203 LTD (FEI: 3007019930) has 4 FDA import refusal record(s) in our database, spanning from 7/26/2011 to 7/26/2011.
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. CareFusion DR 203 LTD's FEI number is 3007019930.
What types of violations has CareFusion DR 203 LTD received?
CareFusion DR 203 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 CareFusion DR 203 LTD come from?
All FDA import refusal data for CareFusion DR 203 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.