FDA Inspection
Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.)Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.) – FDA Inspection, Feb 19, 2013
Record Details
This FDA Inspection record concerns Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.), with an inspection on February 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 19, 2013
- Product Type
- Devices
View Company Profile
ID · 4ccfc52a-6df1-4432-926e-a728d3b2a665
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 816055
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.)
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 30, 2026 | Not classified | Minneapolis District Office | |
| April 24, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 18, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 17, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 23, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Synovis Life Technologies, Inc. (sub. of Baxter Int'l, Inc.)
- FDA Inspection 1339918 - 2026-09-30
- FDA Inspection 1087290 - 2019-04-24
- FDA Inspection 991765 - 2016-10-18
- FDA Inspection 933831 - 2015-06-17
- FDA Inspection 740649 - 2011-08-23
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