FDA Inspection
CareFusion 303, Inc.CareFusion 303, Inc. – FDA Inspection, Sep 29, 2014
Record Details
This FDA Inspection record concerns CareFusion 303, Inc., with an inspection on September 29, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- CareFusion 303, Inc.
- Inspection Date
- September 29, 2014
- Product Type
- Devices
View Company Profile
ID · 7349c143-674f-43ca-8951-4ab31502483c
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 893045
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of CareFusion 303, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2024 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 10, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 6, 2020 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 6, 2018 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 30, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for CareFusion 303, Inc.
- FDA Inspection 1234100 - 2024-05-22
- FDA Inspection 1166360 - 2022-03-10
- FDA Inspection 1123377 - 2020-04-06
- FDA Inspection 1064813 - 2018-09-06
- FDA Inspection 987844 - 2016-09-30
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