Dismark Gmbh
✅ Low Risk
FEI: 3005550576 • Maur, Zurich • SWITZERLAND
FEI Number
3005550576
Location
Maur, Zurich
Country
SWITZERLANDAddress
Rellikonstrasse 7, , Maur, Zurich, Switzerland
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 |
|---|---|---|---|
| 10/29/2015 | 95REZLASER TRAFFIC SIGNAL, SAFETY, SECURITY, SURVEILLANCE LASER | 341REGISTERED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Dismark Gmbh's FDA import refusal history?
Dismark Gmbh (FEI: 3005550576) has 1 FDA import refusal record(s) in our database, spanning from 10/29/2015 to 10/29/2015.
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. Dismark Gmbh's FEI number is 3005550576.
What types of violations has Dismark Gmbh received?
Dismark Gmbh 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 Dismark Gmbh come from?
All FDA import refusal data for Dismark Gmbh 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.