# Covidien – FDA Inspection, Nov 18, 2008

Source: https://www.keypedia.com/records/fda_inspections/covidien/7c9252e1-da39-4679-bb43-15ef6f882250
Source feed: FDA_Inspections

> FDA inspection 547271 of Covidien, November 18, 2008. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 547271
- Company Name: Covidien
- Inspection Date: 2008-11-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 861417 - 2013-12-16
- FDA Inspection 822909 - 2013-03-14
- FDA Inspection 731620 - 2011-06-16

Company: https://www.keypedia.com/companies/covidien/2ff0de85-c594-426f-a945-1629d8014ee6

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