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Ims Messsysteme Gmbh

⚠️ Moderate Risk

FEI: 3001075080 • Heiligenhaus, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3001075080

📍

Location

Heiligenhaus, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Dieselstr. 55, , Heiligenhaus, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/2/2004
Latest Refusal
11/2/2004
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

471×

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
11/2/2004
95L22LASER PRODUCT FOR NON-MEDICAL USE
47NON STD
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ims Messsysteme Gmbh's FDA import refusal history?

Ims Messsysteme Gmbh (FEI: 3001075080) has 1 FDA import refusal record(s) in our database, spanning from 11/2/2004 to 11/2/2004.

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. Ims Messsysteme Gmbh's FEI number is 3001075080.

What types of violations has Ims Messsysteme Gmbh received?

Ims Messsysteme 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 Ims Messsysteme Gmbh come from?

All FDA import refusal data for Ims Messsysteme 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.