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Ferro Pharma Kft.

⚠️ Moderate Risk

FEI: 3003789447 • Doc • HUNGARY

FEI

FEI Number

3003789447

📍

Location

Doc

🇭🇺

Country

HUNGARY
🏢

Address

Erdosor 13, , Doc, , Hungary

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/18/2006
Latest Refusal
1/18/2006
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

1151×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

Refusal History

DateProductViolationsDivision
1/18/2006
65CAR99NUTRIENT/TONIC N.E.C.
115DR QUALITY
223FALSE
New York District Office (NYK-DO)

Frequently Asked Questions

What is Ferro Pharma Kft.'s FDA import refusal history?

Ferro Pharma Kft. (FEI: 3003789447) has 1 FDA import refusal record(s) in our database, spanning from 1/18/2006 to 1/18/2006.

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. Ferro Pharma Kft.'s FEI number is 3003789447.

What types of violations has Ferro Pharma Kft. received?

Ferro Pharma Kft. has been cited for 2 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 Ferro Pharma Kft. come from?

All FDA import refusal data for Ferro Pharma Kft. 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.