FDA Inspection
Covidien, PLCCovidien, PLC – FDA Inspection, Sep 8, 2017
Record Details
This FDA Inspection record concerns Covidien, PLC, with an inspection on September 8, 2017, issued by the Denver District Office, covering medical devices & rad health.
- Company
- Covidien, PLC
- Inspection Date
- September 8, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Denver District Office
View Company Profile
ID · 038fb67e-cc0e-4a6e-9538-1280cda2ab68
Inspection Facts
- Inspection number
- 1051939
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Covidien, PLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 10, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 2, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Covidien, PLC
- FDA Inspection 883807 - 2014-06-10
- FDA Inspection 739525 - 2011-08-02
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