FDA Inspection
Covidien, LPCovidien, LP – FDA Inspection, Sep 1, 2009
Record Details
This FDA Inspection record concerns Covidien, LP, with an inspection on September 1, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Covidien, LP
- Inspection Date
- September 1, 2009
- Product Type
- Devices
View Company Profile
ID · 6d0eb5a2-f67e-4209-a416-a543847a4283
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 611013
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Covidien, LP
8| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2024 | Not classified | New England District Office | |
| February 28, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 1, 2017 | Not classified | New England District Office | |
| August 14, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 6, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Covidien, LP
- FDA Inspection 1255834 - 2024-11-21
- FDA Inspection 1118427 - 2020-02-28
- FDA Inspection 1049809 - 2017-09-01
- FDA Inspection 891371 - 2014-08-14
- FDA Inspection 812526 - 2012-12-06
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