# FDA Inspection 949188 - Pulsar Vascular Inc. - November 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/6908b288-579d-4b14-bd0a-e7f0199d4431
Source feed: FDA_Inspections

> FDA Inspection 949188 for Pulsar Vascular Inc. on November 13, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 949188
- Company Name: Pulsar Vascular Inc.
- Inspection Date: 2015-11-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1003264 - 2017-03-01](https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/f06ca2b3-d456-43fb-ad20-be6f378bcee6)
- [FDA Inspection 991330 - 2016-09-15](https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/d35be9f9-d1b5-4199-9fb8-f773fc3f0800)
- [FDA Inspection 949188 - 2015-11-13](https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/86727a1c-f9cb-463c-ad01-72890488bccf)

Company: https://www.keypedia.com/companies/pulsar-vascular-inc/00ff4ec5-fe9c-411c-bec0-7e55b86f5d24

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