FDA Inspection
Terumo Cardiovascular Systems CorporationTerumo Cardiovascular Systems Corporation – FDA Inspection, Feb 11, 2009
Record Details
This FDA Inspection record concerns Terumo Cardiovascular Systems Corporation, with an inspection on February 11, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 11, 2009
- Product Type
- Devices
View Company Profile
ID · cc220f99-d59b-437a-80c0-75a7eb6262b7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 561886
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Terumo Cardiovascular Systems Corporation
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 16, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 16, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 16, 2018 | Not classified | Baltimore District Office | |
| September 15, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 17, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Terumo Cardiovascular Systems Corporation
- FDA Inspection 1229027 - 2024-02-16
- FDA Inspection 1192936 - 2022-12-16
- FDA Inspection 1080087 - 2018-02-16
- FDA Inspection 986107 - 2016-09-15
- FDA Inspection 832532 - 2013-05-17
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