# FDA Inspection 792561 - Covidien LP - July 20, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/covidien-lp/dda8a09a-e5a5-4243-831d-90f70d5945f6
Source feed: FDA_Inspections

> FDA Inspection 792561 for Covidien LP on July 20, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 792561
- Company Name: Covidien LP
- Inspection Date: 2012-07-20
- 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.globalkeysolutions.net/companies/covidien-lp/63d22b1b-1374-4530-ab2d-48293cfaee75

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