FDA Inspection
Teleflex Medical, Inc.Teleflex Medical, Inc. – FDA Inspection, Jan 15, 2026
Record Details
This FDA Inspection record concerns Teleflex Medical, Inc., with an inspection on January 15, 2026, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d546d3a4-3189-4dcf-a35d-a9b119a5b0e1
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1247768
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Teleflex Medical, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 2, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 25, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 19, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 15, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 23, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Teleflex Medical, Inc.
- FDA Inspection 999376 - 2017-02-02
- FDA Inspection 892353 - 2014-08-25
- FDA Inspection 791220 - 2012-07-19
- FDA Inspection 680471 - 2010-09-15
- FDA Inspection 567643 - 2009-01-23
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