FDA Inspection
Fresenius Kabi Austria GMBHFresenius Kabi Austria GMBH – FDA Inspection, Apr 1, 2016
Record Details
This FDA Inspection record concerns Fresenius Kabi Austria GMBH, with an inspection on April 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Fresenius Kabi Austria GMBH
- Inspection Date
- April 1, 2016
- Product Type
- Devices
View Company Profile
ID · 6e6daf7c-5413-4b0a-89c1-a26c66183c75
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 969912
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Fresenius Kabi Austria GMBH
12| Date | Classification | Office | Project area |
|---|---|---|---|
| March 21, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 28, 2023 | Not classified | Office of Inspections and Investigations | |
| October 13, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 30, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 19, 2018 | Not classified | Office of Inspections and Investigations |
Other documents for Fresenius Kabi Austria GMBH
- FDA Inspection 1251340 - 2024-03-21
- FDA Inspection 1205334 - 2023-03-28
- FDA Inspection 1207391 - 2022-10-13
- FDA Inspection 1162216 - 2020-01-30
- FDA Inspection 1052462 - 2018-04-19
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