# FDA Inspection 824232 - Covidien, LP - March 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/covidien-lp/a09ae764-1830-40fd-affa-d8a4d572ab05
Source feed: FDA_Inspections

> FDA Inspection 824232 for Covidien, LP on March 26, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824232
- Company Name: Covidien, LP
- Inspection Date: 2013-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 824232 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/covidien-lp/40d824fa-3059-4677-8158-183f9ad567ab)

Company: https://www.keypedia.com/companies/covidien-lp/427fd294-879d-49ff-b6d2-6624ed38c899

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