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Metzler Optik Part

⚠️ Moderate Risk

FEI: 3003291527 • Lorch, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3003291527

📍

Location

Lorch, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Muhlstr. 90, , Lorch, 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
1
Unique Violations
4/5/2002
Latest Refusal
4/5/2002
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

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

Refusal History

DateProductViolationsDivision
4/5/2002
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
235NOT IMPACT
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Metzler Optik Part's FDA import refusal history?

Metzler Optik Part (FEI: 3003291527) has 1 FDA import refusal record(s) in our database, spanning from 4/5/2002 to 4/5/2002.

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. Metzler Optik Part's FEI number is 3003291527.

What types of violations has Metzler Optik Part received?

Metzler Optik Part 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 Metzler Optik Part come from?

All FDA import refusal data for Metzler Optik Part 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.