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Curamed

⚠️ Moderate Risk

FEI: 3002697205 • Vianen ut, Utrecht • NETHERLANDS

FEI

FEI Number

3002697205

📍

Location

Vianen ut, Utrecht

🇳🇱
🏢

Address

Voorstraat 57, , Vianen ut, Utrecht, Netherlands

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
11/10/2009
Latest Refusal
11/10/2009
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3421×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

751×

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
11/10/2009
65LDY16HYDROXYPROPYL CELLULOSE (PROTECTANT)
16DIRECTIONS
342PERSONALRX
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Curamed's FDA import refusal history?

Curamed (FEI: 3002697205) has 1 FDA import refusal record(s) in our database, spanning from 11/10/2009 to 11/10/2009.

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. Curamed's FEI number is 3002697205.

What types of violations has Curamed received?

Curamed has been cited for 3 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 Curamed come from?

All FDA import refusal data for Curamed 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.