# FDA Inspection 892814 - Covidien - August 27, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/covidien/2a1a1a34-57e5-48fd-b72f-a8f24d333f0e
Source feed: FDA_Inspections

> FDA Inspection 892814 for Covidien on August 27, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 892814
- Company Name: Covidien
- Inspection Date: 2014-08-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1073469 - 2018-09-19](https://www.globalkeysolutions.net/records/fda_inspections/covidien/995c6451-1fa4-4ba1-9097-cc5b910523d8)
- [FDA Inspection 991996 - 2016-10-31](https://www.globalkeysolutions.net/records/fda_inspections/covidien/18171b01-0f8d-4e3e-857b-b11a22d1332f)
- [FDA Inspection 649689 - 2010-03-03](https://www.globalkeysolutions.net/records/fda_inspections/covidien/e998c3a3-2a16-4500-b245-78ccdb41ae72)
- [FDA Inspection 649689 - 2010-03-03](https://www.globalkeysolutions.net/records/fda_inspections/covidien/f61b2233-f9ff-4c1a-95c6-e9b43dc27409)

Company: https://www.globalkeysolutions.net/companies/covidien/d00512e5-dda9-4409-9e5d-600eb5667563

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