# FDA Inspection 893843 - Abbott Vascular - August 21, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/abbott-vascular/decb68c8-013b-4eb4-b281-5b73966dc337
Source feed: FDA_Inspections

> FDA Inspection 893843 for Abbott Vascular on August 21, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893843
- Company Name: Abbott Vascular
- Inspection Date: 2014-08-21
- 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 893843 - 2014-08-21](https://www.globalkeysolutions.net/records/fda_inspections/abbott-vascular/e7cfcdd9-8856-49bf-a13a-377dc98e17e1)
- [FDA Inspection 668303 - 2010-06-03](https://www.globalkeysolutions.net/records/fda_inspections/abbott-vascular/b9aba51c-8c5c-4f11-b156-f865d92885e1)
- [FDA Inspection 665884 - 2010-05-27](https://www.globalkeysolutions.net/records/fda_inspections/abbott-vascular/3f561f24-ec0c-4538-a8df-c02e329b5fd5)

Company: https://www.globalkeysolutions.net/companies/abbott-vascular/70ec6b4d-9eb2-4e02-8e3f-666fd4df1027

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