# FDA Inspection 907256 - AbbVie Medical Device Center - December 16, 2014

Source: https://www.keypedia.com/records/fda_inspections/abbvie-medical-device-center/a1f2a524-72b9-4313-a4d5-e8d88da72c35
Source feed: FDA_Inspections

> FDA Inspection 907256 for AbbVie Medical Device Center on December 16, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907256
- Company Name: AbbVie Medical Device Center
- Inspection Date: 2014-12-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 907256 - 2014-12-16](https://www.keypedia.com/records/fda_inspections/abbvie-medical-device-center/cbac5b8c-c94b-4756-ac34-1f0c7dc2e331)

Company: https://www.keypedia.com/companies/abbvie-medical-device-center/1da5a0a2-5560-4323-8e15-bd1e1ab88048

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