# FDA Inspection 803358 - Covidien, LLC - October 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/covidien-llc/52e8a7ae-d482-4d34-8fc4-9193db5ebc26
Source feed: FDA_Inspections

> FDA Inspection 803358 for Covidien, LLC on October 17, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803358
- Company Name: Covidien, LLC
- Inspection Date: 2012-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/covidien-llc/7880d213-f3b7-4a04-9fa1-9f0d32cc7f4c

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