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B & C Group Nv/Sa

⚠️ Moderate Risk

FEI: 3007484571 • Louvain-la-Neuve, Brabant wallon • BELGIUM

FEI

FEI Number

3007484571

📍

Location

Louvain-la-Neuve, Brabant wallon

🇧🇪

Country

BELGIUM
🏢

Address

Granbonpre 11, , Louvain-la-Neuve, Brabant wallon, Belgium

Moderate Risk

FDA Import Risk Assessment

31.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
9/30/2015
Latest Refusal
10/7/2010
Earliest Refusal

Score Breakdown

Violation Severity
58.0×40%
Refusal Volume
25.9×30%
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

1183×

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).

30811×

INVDEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a device for investigational use for which no exemption has been granted as prescribed by Section 520(g)

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
9/30/2015
77KCPSYRINGE, ENT
3081INVDEVICE
Division of Northeast Imports (DNEI)
7/26/2013
80KZHINTRODUCER, SYRINGE NEEDLE
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
11/15/2010
74OFMPHLEBOTOMY BLOOD COLLECTION KIT
118NOT LISTED
New Orleans District Office (NOL-DO)
10/7/2010
57YY99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is B & C Group Nv/Sa's FDA import refusal history?

B & C Group Nv/Sa (FEI: 3007484571) has 4 FDA import refusal record(s) in our database, spanning from 10/7/2010 to 9/30/2015.

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. B & C Group Nv/Sa's FEI number is 3007484571.

What types of violations has B & C Group Nv/Sa received?

B & C Group Nv/Sa 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 B & C Group Nv/Sa come from?

All FDA import refusal data for B & C Group Nv/Sa 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.