# Direx Systems Corp. – FDA Inspection, Oct 8, 2014

Source: https://www.keypedia.com/records/fda_inspections/direx-systems-corp/99bd4d3e-fe7a-4ca9-a8e5-f874d4edc178
Source feed: FDA_Inspections

> FDA inspection 899351 of Direx Systems Corp., October 08, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 899351
- Company Name: Direx Systems Corp.
- Inspection Date: 2014-10-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1007613 - 2017-04-12](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/eaac4170-8a4f-4ee0-a185-a0a926d14224)
- [FDA Inspection 775404 - 2012-04-04](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/8aa9d8c5-cd0b-4f0b-8045-746d6c67491f)

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