GREINER BIO-ONE BRASIL
⚠️ Moderate Risk
FEI: 3012860218 • Vila Bertini American • BRAZIL
FEI Number
3012860218
Location
Vila Bertini American
Country
BRAZILAddress
Av. Afonso Pansan 1967 620, , Vila Bertini American, , Brazil
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
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2019 | 74DTQCONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 2/22/2018 | 74DWETUBING, PUMP, CARDIOPULMONARY BYPASS | Division of Southeast Imports (DSEI) | |
| 4/7/2017 | 74DWETUBING, PUMP, CARDIOPULMONARY BYPASS | Division of Southeast Imports (DSEI) | |
| 11/8/2016 | 78KQQTUBING, DIALYSATE (AND CONNECTOR) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is GREINER BIO-ONE BRASIL's FDA import refusal history?
GREINER BIO-ONE BRASIL (FEI: 3012860218) has 4 FDA import refusal record(s) in our database, spanning from 11/8/2016 to 11/22/2019.
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. GREINER BIO-ONE BRASIL's FEI number is 3012860218.
What types of violations has GREINER BIO-ONE BRASIL received?
GREINER BIO-ONE BRASIL 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 GREINER BIO-ONE BRASIL come from?
All FDA import refusal data for GREINER BIO-ONE BRASIL 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.