Siemens Medical Instruments
✅ Low Risk
FEI: 3003019198 • Singapore • SINGAPORE
FEI Number
3003019198
Location
Singapore
Country
SINGAPOREAddress
Pte Ltd (Smi) Blk, , Singapore, , Singapore
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/4/2015 | 77ESDHEARING-AID, AIR-CONDUCTION | 341REGISTERED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Siemens Medical Instruments's FDA import refusal history?
Siemens Medical Instruments (FEI: 3003019198) has 1 FDA import refusal record(s) in our database, spanning from 2/4/2015 to 2/4/2015.
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. Siemens Medical Instruments's FEI number is 3003019198.
What types of violations has Siemens Medical Instruments received?
Siemens Medical Instruments 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 Siemens Medical Instruments come from?
All FDA import refusal data for Siemens Medical Instruments 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.