# FDA Inspection 639004 - Covidien - January 13, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/covidien/876162d0-cb92-49ca-ab9c-99ab05c572c2
Source feed: FDA_Inspections

> FDA Inspection 639004 for Covidien on January 13, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 639004
- Company Name: Covidien
- Inspection Date: 2010-01-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1260161 - 2025-07-16](https://www.globalkeysolutions.net/records/fda_inspections/covidien/319ea92e-abf4-4a91-b287-52d324d8f517)
- [FDA Inspection 1260161 - 2025-07-16](https://www.globalkeysolutions.net/records/fda_inspections/covidien/07d2d10d-e66a-45d2-9483-cd91bda5e5f5)
- [FDA Inspection 917680 - 2015-02-26](https://www.globalkeysolutions.net/records/fda_inspections/covidien/b136d5ae-600e-484e-821b-0aa2483d77f4)
- [FDA Inspection 917680 - 2015-02-26](https://www.globalkeysolutions.net/records/fda_inspections/covidien/fe60d197-4d4f-43ba-871a-a354f828a14b)
- [FDA Inspection 659164 - 2010-04-22](https://www.globalkeysolutions.net/records/fda_inspections/covidien/f4d2f32b-cb0f-4573-8d6c-b445f655bb99)

Company: https://www.globalkeysolutions.net/companies/covidien/e6412dbd-2a1d-4e1c-83d3-1de260dda259

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