SUSS MICROTEC SOLUTIONS GMBH CO
⚠️ Moderate Risk
FEI: 3036162956 • Munich • GERMANY
FEI Number
3036162956
Location
Munich
Country
GERMANYAddress
Schleissheimer Strasse, , Munich, , 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 REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
Frequently Asked Questions
What is SUSS MICROTEC SOLUTIONS GMBH CO's FDA import refusal history?
SUSS MICROTEC SOLUTIONS GMBH CO (FEI: 3036162956) has 2 FDA import refusal record(s) in our database, spanning from 4/23/2025 to 4/23/2025.
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. SUSS MICROTEC SOLUTIONS GMBH CO's FEI number is 3036162956.
What types of violations has SUSS MICROTEC SOLUTIONS GMBH CO received?
SUSS MICROTEC SOLUTIONS GMBH CO 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 SUSS MICROTEC SOLUTIONS GMBH CO come from?
All FDA import refusal data for SUSS MICROTEC SOLUTIONS GMBH CO 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.