# Abbott Vascular – FDA Inspection, Nov 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/abbott-vascular/e5d58afe-dc04-4002-b14d-afdbde356db1
Source feed: FDA_Inspections

> FDA inspection 1031458 of Abbott Vascular, November 15, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031458
- Company Name: Abbott Vascular
- Inspection Date: 2017-11-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

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- FDA Inspection 1109808 - 2018-10-26
- FDA Inspection 1043550 - 2017-09-14
- FDA Inspection 951125 - 2015-12-10

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-a-lane/f6cd3d8d-7de9-45c5-9380-7e0c5de4720e)

Company: https://www.keypedia.com/companies/abbott-vascular/b9a230f1-3cfc-4a75-84cd-4bfddb45afc3

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