Gambro Do Brasil Ltda
✅ Low Risk
FEI: 3003675563 • Sao Paulo, Sao Paulo • BRAZIL
FEI Number
3003675563
Location
Sao Paulo, Sao Paulo
Country
BRAZILAddress
Avenida Engenheiro Luiz Carlos Berrini, 1297, Sao Paulo, Sao Paulo, Brazil
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/12/2008 | 78LKNAUTOMATED BLOOD CELL AND PLASMA SEPARATOR FOR THERAPEUTIC PURPOSES, CENTRIFUGE | 341REGISTERED | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Gambro Do Brasil Ltda's FDA import refusal history?
Gambro Do Brasil Ltda (FEI: 3003675563) has 1 FDA import refusal record(s) in our database, spanning from 9/12/2008 to 9/12/2008.
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. Gambro Do Brasil Ltda's FEI number is 3003675563.
What types of violations has Gambro Do Brasil Ltda received?
Gambro Do Brasil Ltda has been cited for 1 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 Gambro Do Brasil Ltda come from?
All FDA import refusal data for Gambro Do Brasil Ltda 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.