# FDA Inspection 760120 - Abbott Medical - December 22, 2011

Source: https://www.keypedia.com/records/fda_inspections/abbott-medical/027a7d97-eeec-4c6e-bcdb-91f4970a5855
Source feed: FDA_Inspections

> FDA Inspection 760120 for Abbott Medical on December 22, 2011. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 760120
- Company Name: Abbott Medical
- Inspection Date: 2011-12-22
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 863850 - 2014-01-29](https://www.keypedia.com/records/fda_inspections/abbott-medical/7acc37d4-eee9-4107-9e33-a5e968732957)
- [FDA Inspection 863850 - 2014-01-29](https://www.keypedia.com/records/fda_inspections/abbott-medical/6119b3a7-b7aa-4c91-b8d8-dce4f9d9a421)
- [FDA Inspection 807380 - 2012-11-16](https://www.keypedia.com/records/fda_inspections/abbott-medical/c93323f1-2fee-48ce-8d51-336ed7f8067c)
- [FDA Inspection 760120 - 2011-12-22](https://www.keypedia.com/records/fda_inspections/abbott-medical/b5d26670-8f37-4e7b-9957-511aac80be74)

Company: https://www.keypedia.com/companies/abbott-medical/e1c1dbeb-47ba-469d-9e63-f882b86e510b

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