# FDA Inspection 1036260 - Covidien - August 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/covidien/cd35333d-ee03-4370-971c-d2d8f9ffe78d
Source feed: FDA_Inspections

> FDA Inspection 1036260 for Covidien on August 09, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036260
- Company Name: Covidien
- Inspection Date: 2017-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/covidien/b19dc04e-0d0e-489f-94c0-d6d406d65a22

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