Rudolf Storz Gmbh
⚠️ Moderate Risk
FEI: 3002967687 • Emmingen-Liptingen, Baden-Wurttemberg • GERMANY
FEI Number
3002967687
Location
Emmingen-Liptingen, Baden-Wurttemberg
Country
GERMANYAddress
Friedrich-Wohler-Str. 13, , Emmingen-Liptingen, Baden-Wurttemberg, Germany
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
Frequently Asked Questions
What is Rudolf Storz Gmbh's FDA import refusal history?
Rudolf Storz Gmbh (FEI: 3002967687) has 2 FDA import refusal record(s) in our database, spanning from 4/3/2025 to 4/3/2025.
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. Rudolf Storz Gmbh's FEI number is 3002967687.
What types of violations has Rudolf Storz Gmbh received?
Rudolf Storz 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 Rudolf Storz Gmbh come from?
All FDA import refusal data for Rudolf Storz 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.