Jenoptik Laser Optic Systeme
⚠️ Moderate Risk
FEI: 3002561631 • Jena, Thuringia • GERMANY
FEI Number
3002561631
Location
Jena, Thuringia
Country
GERMANYAddress
Goschwitzer Str. 25, , Jena, Thuringia, 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 |
|---|---|---|---|
| 2/11/2009 | 95L22LASER PRODUCT FOR NON-MEDICAL USE | San Francisco District Office (SAN-DO) | |
| 9/5/2006 | 95REQRANGING (GEODIMETER) LASER PRODUCTS, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS | 476NO REGISTR | Cincinnati District Office (CIN-DO) |
| 1/6/2004 | 95L22LASER PRODUCT FOR NON-MEDICAL USE | 47NON STD | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Jenoptik Laser Optic Systeme's FDA import refusal history?
Jenoptik Laser Optic Systeme (FEI: 3002561631) has 3 FDA import refusal record(s) in our database, spanning from 1/6/2004 to 2/11/2009.
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. Jenoptik Laser Optic Systeme's FEI number is 3002561631.
What types of violations has Jenoptik Laser Optic Systeme received?
Jenoptik Laser Optic Systeme 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 Jenoptik Laser Optic Systeme come from?
All FDA import refusal data for Jenoptik Laser Optic Systeme 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.