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Endo Plus B.V.

⚠️ Moderate Risk

FEI: 3003294921 • Zoetermeer, Zuid-Holland • NETHERLANDS

FEI

FEI Number

3003294921

📍

Location

Zoetermeer, Zuid-Holland

🇳🇱
🏢

Address

Cobaltstraat 41, , Zoetermeer, Zuid-Holland, Netherlands

Moderate Risk

FDA Import Risk Assessment

29.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
3/30/2005
Latest Refusal
2/16/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
6.4×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
3/30/2005
84JXICUFF, NERVE
508NO 510(K)
New Orleans District Office (NOL-DO)
2/16/2002
87MRYAPPLIANCES AND ACCESSORIES, FIXATION, BONE, ABSORBABLE SINGLE/MULTIPLE COMPONENT
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Endo Plus B.V.'s FDA import refusal history?

Endo Plus B.V. (FEI: 3003294921) has 2 FDA import refusal record(s) in our database, spanning from 2/16/2002 to 3/30/2005.

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. Endo Plus B.V.'s FEI number is 3003294921.

What types of violations has Endo Plus B.V. received?

Endo Plus B.V. 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 Endo Plus B.V. come from?

All FDA import refusal data for Endo Plus B.V. 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.