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ABZ PHARMA GMBH

⚠️ High Risk

FEI: 3013225813 • Ulm, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3013225813

📍

Location

Ulm, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Graf-Arco-Str. 3, , Ulm, Baden-Wurttemberg, Germany

High Risk

FDA Import Risk Assessment

53.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
2/23/2024
Latest Refusal
8/20/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
47.3×20%
Frequency
11.9×10%
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

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
2/23/2024
66TCY01ALLOPURINOL (XANTHINE OXIDASE INHIBITOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
66SDA05FLUNARIZINE HCL (VASODILATOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/20/2021
62OCA05RAMIPRIL (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ABZ PHARMA GMBH's FDA import refusal history?

ABZ PHARMA GMBH (FEI: 3013225813) has 3 FDA import refusal record(s) in our database, spanning from 8/20/2021 to 2/23/2024.

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. ABZ PHARMA GMBH's FEI number is 3013225813.

What types of violations has ABZ PHARMA GMBH received?

ABZ PHARMA 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 ABZ PHARMA GMBH come from?

All FDA import refusal data for ABZ PHARMA 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.