# FDA Inspection 796052 - Abbott Ireland Diagnostics Division - August 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/abbott-ireland-diagnostics-division/7bcf8791-f1b7-4c9c-9a29-d0dc60853029
Source feed: FDA_Inspections

> FDA Inspection 796052 for Abbott Ireland Diagnostics Division on August 30, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 796052
- Company Name: Abbott Ireland Diagnostics Division
- Inspection Date: 2012-08-30
- 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 796052 - 2012-08-30](https://www.keypedia.com/records/fda_inspections/abbott-ireland-diagnostics-division/17fee2a9-f898-4512-a155-a30e0a94f9ac)

Company: https://www.keypedia.com/companies/abbott-ireland-diagnostics-division/80b65c10-bc39-43f5-9c7e-bdcae6b34685

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