# FDA Inspection 611013 - Covidien, LP - September 01, 2009

Source: https://www.keypedia.com/records/fda_inspections/covidien-lp/310e1f96-edbe-48b5-88be-b80ccbe5e8f9
Source feed: FDA_Inspections

> FDA Inspection 611013 for Covidien, LP on September 01, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611013
- Company Name: Covidien, LP
- Inspection Date: 2009-09-01
- 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-lp/d641f53a-9d4b-4b04-aa52-a7e3fbed7428

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