Exbio Praha A S
⚠️ Moderate Risk
FEI: 3008794764 • Vestec • CZECH REPUBLIC
FEI Number
3008794764
Location
Vestec
Country
CZECH REPUBLICAddress
Nad Safinou Ii 341, , Vestec, , Czech Republic
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
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/23/2022 | 88PPMGENERAL PURPOSE REAGENT | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 9/7/2018 | 57YH99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C. | 223FALSE | Division of Southeast Imports (DSEI) |
| 9/7/2018 | 88OTURESEARCH USE ONLY/PATHOLOGY | 223FALSE | Division of Southeast Imports (DSEI) |
| 9/7/2018 | 88OTURESEARCH USE ONLY/PATHOLOGY | 223FALSE | Division of Southeast Imports (DSEI) |
| 9/7/2018 | 88OTURESEARCH USE ONLY/PATHOLOGY | 223FALSE | Division of Southeast Imports (DSEI) |
| 9/7/2018 | 57UL99BLOOD DERIVIATIVES, N.E.C | 223FALSE | Division of Southeast Imports (DSEI) |
| 1/13/2016 | 88NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS | New Orleans District Office (NOL-DO) | |
| 1/13/2016 | 75PFTREAGENTS FOR MOLECULAR DIAGNOSTIC TEST SYSTEMS | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Exbio Praha A S's FDA import refusal history?
Exbio Praha A S (FEI: 3008794764) has 8 FDA import refusal record(s) in our database, spanning from 1/13/2016 to 7/23/2022.
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. Exbio Praha A S's FEI number is 3008794764.
What types of violations has Exbio Praha A S received?
Exbio Praha A S 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 Exbio Praha A S come from?
All FDA import refusal data for Exbio Praha A S 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.