QUINTENZ HYBRIDTECHNIK GMBH
✅ Low Risk
FEI: 3010232390 • Neuried, Bavaria • GERMANY
FEI Number
3010232390
Location
Neuried, Bavaria
Country
GERMANYAddress
Eichenstr. 15, , Neuried, Bavaria, Germany
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
3904
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/30/2024 | 87OLOORTHOPEDIC STEREOTAXIC INSTRUMENT | 39043904 | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is QUINTENZ HYBRIDTECHNIK GMBH's FDA import refusal history?
QUINTENZ HYBRIDTECHNIK GMBH (FEI: 3010232390) has 1 FDA import refusal record(s) in our database, spanning from 7/30/2024 to 7/30/2024.
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. QUINTENZ HYBRIDTECHNIK GMBH's FEI number is 3010232390.
What types of violations has QUINTENZ HYBRIDTECHNIK GMBH received?
QUINTENZ HYBRIDTECHNIK 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 QUINTENZ HYBRIDTECHNIK GMBH come from?
All FDA import refusal data for QUINTENZ HYBRIDTECHNIK 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.