Bio-Rad Laboratories
⚠️ Moderate Risk
FEI: 3002889627 • Marnes-La-Coquette, Hauts-de-Seine • FRANCE
FEI Number
3002889627
Location
Marnes-La-Coquette, Hauts-de-Seine
Country
FRANCEAddress
3 Boulevard Raymond Poincare, , Marnes-La-Coquette, Hauts-de-Seine, France
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
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).
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).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/7/2014 | 82MZFTEST, HIV DETECTION | New York District Office (NYK-DO) | |
| 1/10/2006 | 90MYNANALYZER, MEDICAL IMAGE | Florida District Office (FLA-DO) | |
| 1/18/2005 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 1/18/2005 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) | |
| 11/25/2003 | 80LDQDEVICE, GENERAL MEDICAL | 237NO PMA | Florida District Office (FLA-DO) |
| 11/25/2003 | 80LDQDEVICE, GENERAL MEDICAL | 237NO PMA | Florida District Office (FLA-DO) |
| 9/20/2003 | 80LDQDEVICE, GENERAL MEDICAL | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Bio-Rad Laboratories's FDA import refusal history?
Bio-Rad Laboratories (FEI: 3002889627) has 7 FDA import refusal record(s) in our database, spanning from 9/20/2003 to 11/7/2014.
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. Bio-Rad Laboratories's FEI number is 3002889627.
What types of violations has Bio-Rad Laboratories received?
Bio-Rad Laboratories 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 Bio-Rad Laboratories come from?
All FDA import refusal data for Bio-Rad Laboratories 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.