# Cardiva Medical, Inc. – FDA Inspection, May 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/be7890ab-e800-406f-8eb6-3f4779213554
Source feed: FDA_Inspections

> FDA inspection 1014545 of Cardiva Medical, Inc., May 10, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014545
- Company Name: Cardiva Medical, Inc.
- Inspection Date: 2017-05-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1211273 - 2023-07-21](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/ec7bae42-612c-4325-ad04-530d283ebafd)
- FDA Inspection 1084157 - 2019-03-14
- FDA Inspection 871451 - 2014-03-25
- FDA Inspection 809441 - 2012-11-19
- FDA Inspection 807691 - 2012-10-30

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/cardiva-medical-inc/d2c13d97-eb8f-4b56-bcf4-052d6081107f

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