Gentaur Molecular Prod Bvba
⚠️ Moderate Risk
FEI: 3005984311 • Kampenhout, Vlaams-Brabant • BELGIUM
FEI Number
3005984311
Location
Kampenhout, Vlaams-Brabant
Country
BELGIUMAddress
Voortstraat 49, , Kampenhout, Vlaams-Brabant, Belgium
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/26/2021 | 83QMNCOVID-19 MULTI-ANALYTE ANTIGEN DEVICE | Division of Southeast Imports (DSEI) | |
| 2/16/2021 | 83QKOREAGENT, CORONAVIRUS SEROLOGICAL | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 2/8/2021 | 83QKOREAGENT, CORONAVIRUS SEROLOGICAL | 508NO 510(K) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Gentaur Molecular Prod Bvba's FDA import refusal history?
Gentaur Molecular Prod Bvba (FEI: 3005984311) has 3 FDA import refusal record(s) in our database, spanning from 2/8/2021 to 2/26/2021.
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. Gentaur Molecular Prod Bvba's FEI number is 3005984311.
What types of violations has Gentaur Molecular Prod Bvba received?
Gentaur Molecular Prod Bvba has been cited for 4 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 Gentaur Molecular Prod Bvba come from?
All FDA import refusal data for Gentaur Molecular Prod Bvba 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.