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Aeskulab Diagnostika

⚠️ Moderate Risk

FEI: 3003674265 • Wendelsheim, Rhineland-Palatinate • GERMANY

FEI

FEI Number

3003674265

📍

Location

Wendelsheim, Rhineland-Palatinate

🇩🇪

Country

GERMANY
🏢

Address

Mikro-Forum-Ring 2, , Wendelsheim, Rhineland-Palatinate, 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
8/31/2004
Latest Refusal
8/31/2004
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

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
8/31/2004
83LKQANTIBODY IGM,IF, CYTOMEGALOVIRUS VIRUS
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Aeskulab Diagnostika's FDA import refusal history?

Aeskulab Diagnostika (FEI: 3003674265) has 1 FDA import refusal record(s) in our database, spanning from 8/31/2004 to 8/31/2004.

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. Aeskulab Diagnostika's FEI number is 3003674265.

What types of violations has Aeskulab Diagnostika received?

Aeskulab Diagnostika 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 Aeskulab Diagnostika come from?

All FDA import refusal data for Aeskulab Diagnostika 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.