SKAN AG
⚠️ Moderate Risk
FEI: 3019763873 • Allschwil • SWITZERLAND
FEI Number
3019763873
Location
Allschwil
Country
SWITZERLANDAddress
Kreuzstrasse 5, , Allschwil, , Switzerland
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
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/11/2023 | 79GEXPOWERED LASER SURGICAL INSTRUMENTS | 126FAILS STD | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SKAN AG's FDA import refusal history?
SKAN AG (FEI: 3019763873) has 1 FDA import refusal record(s) in our database, spanning from 10/11/2023 to 10/11/2023.
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. SKAN AG's FEI number is 3019763873.
What types of violations has SKAN AG received?
SKAN AG 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 SKAN AG come from?
All FDA import refusal data for SKAN AG 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.