# FDA Inspection 982024 - Covidien (formerly Mallinckrodt Medical) - July 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/covidien-formerly-mallinckrodt-medical/2c6602b0-baf7-45ca-a8ca-500c378b04cf
Source feed: FDA_Inspections

> FDA Inspection 982024 for Covidien (formerly Mallinckrodt Medical) on July 21, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982024
- Company Name: Covidien (formerly Mallinckrodt Medical)
- Inspection Date: 2016-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 982024 - 2016-07-21](https://www.keypedia.com/records/fda_inspections/covidien-formerly-mallinckrodt-medical/747378d7-daf5-45ed-ae9e-f25afa3eb3ec)

Company: https://www.keypedia.com/companies/covidien-formerly-mallinckrodt-medical/fdc33dca-5944-4120-acad-87c0b0606e63

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