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Dr Honle Ag Uv Technology

⚠️ Moderate Risk

FEI: 3005890002 • Grafelfing, Bavaria • GERMANY

FEI

FEI Number

3005890002

📍

Location

Grafelfing, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Postfach 1510, , Grafelfing, Bavaria, Germany

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/13/2009
Latest Refusal
10/13/2009
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

Refusal History

DateProductViolationsDivision
10/13/2009
79MXGLAMP, UVC (FOR TREATING SKIN AND WOUNDS)
126FAILS STD
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dr Honle Ag Uv Technology's FDA import refusal history?

Dr Honle Ag Uv Technology (FEI: 3005890002) has 1 FDA import refusal record(s) in our database, spanning from 10/13/2009 to 10/13/2009.

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. Dr Honle Ag Uv Technology's FEI number is 3005890002.

What types of violations has Dr Honle Ag Uv Technology received?

Dr Honle Ag Uv Technology 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 Dr Honle Ag Uv Technology come from?

All FDA import refusal data for Dr Honle Ag Uv Technology 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.