FDA Inspection
Fresenius Kabi WarrendaleFresenius Kabi Warrendale – FDA Inspection, Sep 14, 2017
Record Details
This FDA Inspection record concerns Fresenius Kabi Warrendale, with an inspection on September 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b981ba4b-be16-4378-b1bc-1af55ea724f7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1030393
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Fresenius Kabi Warrendale
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2024 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 5, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 20, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 27, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 7, 2008 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Fresenius Kabi Warrendale
- FDA Inspection 1237140 - 2024-04-16
- FDA Inspection 924837 - 2015-05-05
- FDA Inspection 812876 - 2012-12-20
- FDA Inspection 735611 - 2011-05-27
- FDA Inspection 541136 - 2008-10-07
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