# FDA Inspection 1003264 - Pulsar Vascular Inc. - March 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/f06ca2b3-d456-43fb-ad20-be6f378bcee6
Source feed: FDA_Inspections

> FDA Inspection 1003264 for Pulsar Vascular Inc. on March 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003264
- Company Name: Pulsar Vascular Inc.
- Inspection Date: 2017-03-01
- 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 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)
- [FDA Inspection 949188 - 2015-11-13](https://www.keypedia.com/records/fda_inspections/pulsar-vascular-inc/6908b288-579d-4b14-bd0a-e7f0199d4431)

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