# Covidien LP – FDA Inspection, Aug 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/covidien-lp/a65b1270-3133-4887-a0d1-e3fdc4324bb1
Source feed: FDA_Inspections

> FDA inspection 844859 of Covidien LP, August 15, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 844859
- Company Name: Covidien LP
- Inspection Date: 2013-08-15
- 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: 3

## Related Documents

- [FDA Inspection 1191674 - 2022-11-18](https://www.keypedia.com/records/fda_inspections/covidien-lp/7e2d98c2-fd64-42ed-82b0-cfc26c4e55e5)
- [FDA Inspection 1029477 - 2017-05-19](https://www.keypedia.com/records/fda_inspections/covidien-lp/2cd73d82-0751-4cdf-ab11-aa9dbe00beb6)
- [FDA Inspection 1034600 - 2017-05-17](https://www.keypedia.com/records/fda_inspections/covidien-lp/fbb361f2-41fa-4eb9-b6a2-342d752b0763)
- FDA Inspection 792561 - 2012-07-20
- FDA Inspection 778312 - 2012-04-09

Company: https://www.keypedia.com/companies/covidien-lp/63d22b1b-1374-4530-ab2d-48293cfaee75

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