# FDA Inspection 1180857 - Covidien - September 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/covidien/5819ceba-1e50-4450-be57-e46414596bd4
Source feed: FDA_Inspections

> FDA Inspection 1180857 for Covidien on September 08, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180857
- Company Name: Covidien
- Inspection Date: 2022-09-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 728020 - 2011-05-12](https://www.keypedia.com/records/fda_inspections/covidien/368fc21e-0195-481f-8856-3faf22486727)
- [FDA Inspection 728020 - 2011-05-12](https://www.keypedia.com/records/fda_inspections/covidien/4d4a1c60-beed-41e2-93de-7cff51687d86)
- [FDA Inspection 668310 - 2010-05-27](https://www.keypedia.com/records/fda_inspections/covidien/9b03004f-247a-4681-9d08-0da541cce5e1)

Company: https://www.keypedia.com/companies/covidien/3a39e019-36f0-4d2e-9e50-44af851b8c50

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