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Bader Europe Group S.L.

✅ Low Risk

FEI: 3011463624 • Nigran • SPAIN

FEI

FEI Number

3011463624

📍

Location

Nigran

🇪🇸

Country

SPAIN
🏢

Address

Rua Dos Padrons No 3, , Nigran, , Spain

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
3
Unique Violations
6/10/2015
Latest Refusal
6/10/2015
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

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
6/10/2015
74NSAOVER-THE-COUNTER AUTOMATED EXTERNAL DEFIBRILLATOR
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Bader Europe Group S.L.'s FDA import refusal history?

Bader Europe Group S.L. (FEI: 3011463624) has 1 FDA import refusal record(s) in our database, spanning from 6/10/2015 to 6/10/2015.

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. Bader Europe Group S.L.'s FEI number is 3011463624.

What types of violations has Bader Europe Group S.L. received?

Bader Europe Group S.L. 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 Bader Europe Group S.L. come from?

All FDA import refusal data for Bader Europe Group S.L. 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.