Multi-Lite Lichttechnik Gmbh
⚠️ Moderate Risk
FEI: 3005013880 • Hamburg, Hamburg • GERMANY
FEI Number
3005013880
Location
Hamburg, Hamburg
Country
GERMANYAddress
Holstenhofweg 60, , Hamburg, Hamburg, 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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/15/2014 | 95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS | 476NO REGISTR | San Francisco District Office (SAN-DO) |
| 10/15/2014 | 95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS | 476NO REGISTR | San Francisco District Office (SAN-DO) |
| 10/15/2014 | 95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS | 476NO REGISTR | San Francisco District Office (SAN-DO) |
| 6/2/2011 | 95RDYMETAL HALIDE LAMP, MERCURY VAPOR LAMPS | 47NON STD | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Multi-Lite Lichttechnik Gmbh's FDA import refusal history?
Multi-Lite Lichttechnik Gmbh (FEI: 3005013880) has 4 FDA import refusal record(s) in our database, spanning from 6/2/2011 to 10/15/2014.
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. Multi-Lite Lichttechnik Gmbh's FEI number is 3005013880.
What types of violations has Multi-Lite Lichttechnik Gmbh received?
Multi-Lite Lichttechnik Gmbh 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 Multi-Lite Lichttechnik Gmbh come from?
All FDA import refusal data for Multi-Lite Lichttechnik 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.