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Eltromat

⚠️ Moderate Risk

FEI: 3003657740 • Leopoldshohe, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3003657740

📍

Location

Leopoldshohe, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Postfach 1163, , Leopoldshohe, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
7/3/2003
Latest Refusal
7/3/2003
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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.

Refusal History

DateProductViolationsDivision
7/3/2003
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
47NON STD
Baltimore District Office (BLT-DO)
7/3/2003
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
47NON STD
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Eltromat's FDA import refusal history?

Eltromat (FEI: 3003657740) has 2 FDA import refusal record(s) in our database, spanning from 7/3/2003 to 7/3/2003.

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. Eltromat's FEI number is 3003657740.

What types of violations has Eltromat received?

Eltromat 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 Eltromat come from?

All FDA import refusal data for Eltromat 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.