# Covidien, LLC – FDA Inspection, Jun 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/covidien-llc/fccf1fc3-dce5-4335-81ab-748307d2e944
Source feed: FDA_Inspections

> FDA inspection 668848 of Covidien, LLC, June 15, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 668848
- Company Name: Covidien, LLC
- Inspection Date: 2010-06-15
- 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: 4

## Related Documents

- [FDA Inspection 1031445 - 2017-05-10](https://www.keypedia.com/records/fda_inspections/covidien-llc/1c6ebb5d-e51c-409b-ab14-8e464a882551)
- FDA Inspection 984992 - 2016-09-20
- FDA Inspection 932211 - 2015-06-03
- FDA Inspection 834276 - 2013-05-16
- FDA Inspection 782057 - 2012-05-17

Company: https://www.keypedia.com/companies/covidien-llc/0787a7fa-505a-419e-afe8-8c492f5cf1d8

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