# FDA Inspection 1000893 - QSPEX Technologies Inc. - January 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/qspex-technologies-inc/2b63b68a-0a5b-4779-baaa-466d68f4a39d
Source feed: FDA_Inspections

> FDA Inspection 1000893 for QSPEX Technologies Inc. on January 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000893
- Company Name: QSPEX Technologies Inc.
- Inspection Date: 2017-01-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/qspex-technologies-inc/e36f05be-f0bf-4c32-862f-20cc5b53f17c

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