# FDA Inspection 861417 - Covidien - December 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/covidien/7b5ab9e0-9ffb-4aa6-9585-d811aa1ea313
Source feed: FDA_Inspections

> FDA Inspection 861417 for Covidien on December 16, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 861417
- Company Name: Covidien
- Inspection Date: 2013-12-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 861417 - 2013-12-16](https://www.keypedia.com/records/fda_inspections/covidien/49d7d402-06bd-4bea-83d3-60e371003ae8)
- [FDA Inspection 822909 - 2013-03-14](https://www.keypedia.com/records/fda_inspections/covidien/520982ba-6bdc-43ca-be2c-0b8cb9895c05)
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- [FDA Inspection 731620 - 2011-06-16](https://www.keypedia.com/records/fda_inspections/covidien/250d8f71-27b9-4638-89d9-e9b81fc721cc)
- [FDA Inspection 731620 - 2011-06-16](https://www.keypedia.com/records/fda_inspections/covidien/c90dd86a-b8b6-4cd3-9041-1886ccf001f0)

Company: https://www.keypedia.com/companies/covidien/2ff0de85-c594-426f-a945-1629d8014ee6

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7