Fresenius Kabi Austria GMBH
⚠️ Moderate Risk
FEI: 3003708554 • Graz, Styria • AUSTRIA
FEI Number
3003708554
Location
Graz, Styria
Country
AUSTRIAAddress
Hafnerstrase 36, , Graz, Styria, Austria
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.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/11/2022 | 80PGOANTI-STICK GLASS SYRINGE | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 7/31/2017 | 60QCK84PROPOFOL (ANESTHETIC) | Division of Northern Border Imports (DNBI) | |
| 7/31/2017 | 60QCK84PROPOFOL (ANESTHETIC) | Division of Northern Border Imports (DNBI) | |
| 7/27/2011 | 63ACL11IBANDRONATE SODIUM | 75UNAPPROVED | New York District Office (NYK-DO) |
| 10/17/2009 | 64LIY19DEXAMETHASONE (GLUCOCORTICOID) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Fresenius Kabi Austria GMBH's FDA import refusal history?
Fresenius Kabi Austria GMBH (FEI: 3003708554) has 5 FDA import refusal record(s) in our database, spanning from 10/17/2009 to 7/11/2022.
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. Fresenius Kabi Austria GMBH's FEI number is 3003708554.
What types of violations has Fresenius Kabi Austria GMBH received?
Fresenius Kabi Austria GMBH 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 Fresenius Kabi Austria GMBH come from?
All FDA import refusal data for Fresenius Kabi Austria GMBH 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.