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EXCELITAS NOBLELIGHT GMBH

⚠️ High Risk

FEI: 3030452505 • Alzenau, Bavaria • GERMANY

FEI

FEI Number

3030452505

📍

Location

Alzenau, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Carl-Zeiss-Str. 4, , Alzenau, Bavaria, Germany

High Risk

FDA Import Risk Assessment

51.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
1
Unique Violations
10/10/2025
Latest Refusal
10/10/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
80.7×20%
Frequency
20.0×10%
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

472×

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

DateProductViolationsDivision
10/10/2025
95RGWUV/IR RESEARCH PRODUCT, GENERAL OPTICAL, NON-MEDICAL
47NON STD
Division of Southeast Imports (DSEI)
10/10/2025
95RGWUV/IR RESEARCH PRODUCT, GENERAL OPTICAL, NON-MEDICAL
47NON STD
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is EXCELITAS NOBLELIGHT GMBH's FDA import refusal history?

EXCELITAS NOBLELIGHT GMBH (FEI: 3030452505) has 2 FDA import refusal record(s) in our database, spanning from 10/10/2025 to 10/10/2025.

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. EXCELITAS NOBLELIGHT GMBH's FEI number is 3030452505.

What types of violations has EXCELITAS NOBLELIGHT GMBH received?

EXCELITAS NOBLELIGHT GMBH 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 EXCELITAS NOBLELIGHT GMBH come from?

All FDA import refusal data for EXCELITAS NOBLELIGHT 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.