ImportRefusal LogoImportRefusal

Denk Pharma

⚠️ Moderate Risk

FEI: 3011052494 • Munchen, Bayern • GERMANY

FEI

FEI Number

3011052494

📍

Location

Munchen, Bayern

🇩🇪

Country

GERMANY
🏢

Address

Prinzregentenstrase 79, , Munchen, Bayern, Germany

Moderate Risk

FDA Import Risk Assessment

43.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
9/7/2018
Latest Refusal
12/1/2014
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
8.0×10%
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

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
9/7/2018
61PCA26METFORMIN (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/1/2014
61PCB26METFORMIN (ANTI-DIABETIC)
75UNAPPROVED
Florida District Office (FLA-DO)
12/1/2014
65PCB03TAMSULOSIN HCL (REGULATOR)
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Denk Pharma's FDA import refusal history?

Denk Pharma (FEI: 3011052494) has 3 FDA import refusal record(s) in our database, spanning from 12/1/2014 to 9/7/2018.

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. Denk Pharma's FEI number is 3011052494.

What types of violations has Denk Pharma received?

Denk Pharma 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 Denk Pharma come from?

All FDA import refusal data for Denk Pharma 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.