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Lohmann X-Ray

⚠️ Moderate Risk

FEI: 1000162685 • Leverkusen • GERMANY

FEI

FEI Number

1000162685

📍

Location

Leverkusen

🇩🇪

Country

GERMANY
🏢

Address

Hardenbergstrasse !, , Leverkusen, , Germany

Moderate Risk

FDA Import Risk Assessment

34.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
2
Unique Violations
10/6/2003
Latest Refusal
10/6/2003
Earliest Refusal

Score Breakdown

Violation Severity
66.7×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
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.

4761×

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

DateProductViolationsDivision
10/6/2003
94V05CATHODE RAY TUBE
47NON STD
476NO REGISTR
Chicago District Office (CHI-DO)
10/6/2003
94V05CATHODE RAY TUBE
47NON STD
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Lohmann X-Ray's FDA import refusal history?

Lohmann X-Ray (FEI: 1000162685) has 2 FDA import refusal record(s) in our database, spanning from 10/6/2003 to 10/6/2003.

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. Lohmann X-Ray's FEI number is 1000162685.

What types of violations has Lohmann X-Ray received?

Lohmann X-Ray 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 Lohmann X-Ray come from?

All FDA import refusal data for Lohmann X-Ray 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.