# Direx Systems Corp. – FDA Inspection, Apr 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/direx-systems-corp/eaac4170-8a4f-4ee0-a185-a0a926d14224
Source feed: FDA_Inspections

> FDA inspection 1007613 of Direx Systems Corp., April 12, 2017. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007613
- Company Name: Direx Systems Corp.
- Inspection Date: 2017-04-12
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 899351 - 2014-10-08](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/99bd4d3e-fe7a-4ca9-a8e5-f874d4edc178)
- [FDA Inspection 775404 - 2012-04-04](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/8aa9d8c5-cd0b-4f0b-8045-746d6c67491f)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/direx-systems-corp/032cf35f-f13b-4380-8bf7-089beb0314d8

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