FDA Inspection
Fresenius U.S.A. ManufacturingFresenius U.S.A. Manufacturing – FDA Inspection, May 8, 2023
Record Details
This FDA Inspection record concerns Fresenius U.S.A. Manufacturing, with an inspection on May 8, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d76d9ac0-8aa1-4b15-bbc5-0fc591907b95
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1206544
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Fresenius U.S.A. Manufacturing
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 30, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 27, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 15, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Fresenius U.S.A. Manufacturing
- FDA Inspection 1016670 - 2017-06-30
- FDA Inspection 809863 - 2012-12-27
- FDA Inspection 667215 - 2010-06-15
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