Lap GmbH Laser Applikationen
⚠️ Moderate Risk
FEI: 3000253133 • LUENEBURG, Lower Saxony • GERMANY
FEI Number
3000253133
Location
LUENEBURG, Lower Saxony
Country
GERMANYAddress
Zeppelinstr. 23, , LUENEBURG, Lower Saxony, 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
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/6/2017 | 90IWEMONITOR, PATIENT POSITION, LIGHT-BEAM | 47NON STD | Division of Southeast Imports (DSEI) |
| 12/6/2017 | 90IWEMONITOR, PATIENT POSITION, LIGHT-BEAM | 47NON STD | Division of Southeast Imports (DSEI) |
| 12/6/2017 | 90IWEMONITOR, PATIENT POSITION, LIGHT-BEAM | 47NON STD | Division of Southeast Imports (DSEI) |
| 11/22/2001 | 95L22LASER PRODUCT FOR NON-MEDICAL USE | 476NO REGISTR | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Lap GmbH Laser Applikationen's FDA import refusal history?
Lap GmbH Laser Applikationen (FEI: 3000253133) has 4 FDA import refusal record(s) in our database, spanning from 11/22/2001 to 12/6/2017.
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. Lap GmbH Laser Applikationen's FEI number is 3000253133.
What types of violations has Lap GmbH Laser Applikationen received?
Lap GmbH Laser Applikationen has been cited for 2 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 Lap GmbH Laser Applikationen come from?
All FDA import refusal data for Lap GmbH Laser Applikationen 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.