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Kneer Gmbh Fenster Und Turen

⚠️ Moderate Risk

FEI: 3009238180 • Westerheim, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3009238180

📍

Location

Westerheim, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Riedstr. 45, , Westerheim, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/6/2012
Latest Refusal
1/6/2012
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

Refusal History

DateProductViolationsDivision
1/6/2012
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Kneer Gmbh Fenster Und Turen's FDA import refusal history?

Kneer Gmbh Fenster Und Turen (FEI: 3009238180) has 1 FDA import refusal record(s) in our database, spanning from 1/6/2012 to 1/6/2012.

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. Kneer Gmbh Fenster Und Turen's FEI number is 3009238180.

What types of violations has Kneer Gmbh Fenster Und Turen received?

Kneer Gmbh Fenster Und Turen 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 Kneer Gmbh Fenster Und Turen come from?

All FDA import refusal data for Kneer Gmbh Fenster Und Turen 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.