# FDA Inspection 940880 - Qspex Technologies, Inc. - September 04, 2015

Source: https://www.keypedia.com/records/fda_inspections/qspex-technologies-inc/59145915-7f87-4d05-869d-4433718209e0
Source feed: FDA_Inspections

> FDA Inspection 940880 for Qspex Technologies, Inc. on September 04, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940880
- Company Name: Qspex Technologies, Inc.
- Inspection Date: 2015-09-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/qspex-technologies-inc/baa19eae-17ea-4ed0-801a-86dd578fba88

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