# Pyrexar Medical, Inc. – FDA Inspection, Sep 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 of Pyrexar Medical, Inc., September 27, 2017. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026744
- Company Name: Pyrexar Medical, Inc.
- Inspection Date: 2017-09-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1169758 - 2022-05-18](https://www.keypedia.com/records/fda_inspections/pyrexar-medical-inc/5b7bacc1-f9d4-4e40-b543-a1db8b70e293)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

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