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Ovamed Gmbh

⚠️ Moderate Risk

FEI: 3004841375 • Barsbuttel, Schleswig-Holstein • GERMANY

FEI

FEI Number

3004841375

📍

Location

Barsbuttel, Schleswig-Holstein

🇩🇪

Country

GERMANY
🏢

Address

Kiebitzhorn 33-35, , Barsbuttel, Schleswig-Holstein, Germany

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/20/2006
Latest Refusal
5/2/2006
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

713×

NO LICENSE

The article is subject to refusal of admission under section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it appears to be a biological product for which a biologics license is not in effect under the Public Health Service Act, Part F, Subpart 1-Biological Products, Section 351(a), and it is not the subject of an Investigational New Drug application that is in effect. Therefore, it appears to be a new drug under 201(p) of the FD&C Act that it is in violation of section 505(a) of the FD&C Act because it lacks a new drug approval and because it is misbranded under section 502(f)(1)of the FD&C Act because it fails to bear adequate directions for use

Refusal History

DateProductViolationsDivision
7/20/2006
57YY99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
71NO LICENSE
New Orleans District Office (NOL-DO)
5/7/2006
57YY99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
71NO LICENSE
New Orleans District Office (NOL-DO)
5/2/2006
57YH99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
71NO LICENSE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ovamed Gmbh's FDA import refusal history?

Ovamed Gmbh (FEI: 3004841375) has 3 FDA import refusal record(s) in our database, spanning from 5/2/2006 to 7/20/2006.

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. Ovamed Gmbh's FEI number is 3004841375.

What types of violations has Ovamed Gmbh received?

Ovamed 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 Ovamed Gmbh come from?

All FDA import refusal data for Ovamed 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.