# Abbott Medical – FDA Inspection, Sep 28, 2012

Source: https://www.keypedia.com/records/fda_inspections/abbott-medical/d8b118e9-9589-4cba-b83a-2ce15c8a0458
Source feed: FDA_Inspections

> FDA inspection 802031 of Abbott Medical, September 28, 2012. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802031
- Company Name: Abbott Medical
- Inspection Date: 2012-09-28
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1122751 - 2018-09-26
- FDA Inspection 967466 - 2016-01-22
- FDA Inspection 696712 - 2010-11-03
- [FDA Inspection 605389 - 2009-07-29](https://www.keypedia.com/records/fda_inspections/abbott-medical/f8558eeb-7bf0-4a63-885f-8c8927b87519)

Company: https://www.keypedia.com/companies/abbott-medical/c5dfe475-e9fc-4fe9-acdd-3c6f76e72626

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