# Covidien – FDA Inspection, May 12, 2011

Source: https://www.keypedia.com/records/fda_inspections/covidien/4d4a1c60-beed-41e2-93de-7cff51687d86
Source feed: FDA_Inspections

> FDA inspection 728020 of Covidien, May 12, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 728020
- Company Name: Covidien
- Inspection Date: 2011-05-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1180857 - 2022-09-08
- FDA Inspection 668310 - 2010-05-27

Company: https://www.keypedia.com/companies/covidien/3a39e019-36f0-4d2e-9e50-44af851b8c50

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