# FDA Inspection 1014545 - Cardiva Medical, Inc. - May 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/5ea09c79-dac5-4c32-97e9-b8cd68b0167b
Source feed: FDA_Inspections

> FDA Inspection 1014545 for Cardiva Medical, Inc. on May 10, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1014545
- Company Name: Cardiva Medical, Inc.
- Inspection Date: 2017-05-10
- 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 1211273 - 2023-07-21](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/ec7bae42-612c-4325-ad04-530d283ebafd)
- [FDA Inspection 1211273 - 2023-07-21](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/a9983b32-97a1-4cd2-85d6-88bf6aa8105f)
- [FDA Inspection 1084157 - 2019-03-14](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/f196b505-5ec5-4feb-8625-50dd6d1542c2)
- [FDA Inspection 1084157 - 2019-03-14](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/edc61621-4c08-403e-816d-da93f421c143)
- [FDA Inspection 1014545 - 2017-05-10](https://www.keypedia.com/records/fda_inspections/cardiva-medical-inc/be7890ab-e800-406f-8eb6-3f4779213554)

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