# FDA Inspection 1026744 - Pyrexar Medical, Inc. - September 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/pyrexar-medical-inc/5d83707b-aefa-4f48-bca3-3e4a014735dc
Source feed: FDA_Inspections

> FDA Inspection 1026744 for Pyrexar Medical, Inc. on September 27, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1026744
- Company Name: Pyrexar Medical, Inc.
- Inspection Date: 2017-09-27
- 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 1169758 - 2022-05-18](https://www.keypedia.com/records/fda_inspections/pyrexar-medical-inc/2a7cea6a-8219-4432-9549-209013b56a48)
- [FDA Inspection 1169758 - 2022-05-18](https://www.keypedia.com/records/fda_inspections/pyrexar-medical-inc/5b7bacc1-f9d4-4e40-b543-a1db8b70e293)
- [FDA Inspection 1026744 - 2017-09-27](https://www.keypedia.com/records/fda_inspections/pyrexar-medical-inc/43f3ea11-2c7c-4f39-9fd3-4ec72669623c)

Company: https://www.keypedia.com/companies/pyrexar-medical-inc/28a81a86-e004-4cab-9d6c-36a492f09349

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