FDA Inspection
Qspex Technologies, Inc.Qspex Technologies, Inc. – FDA Inspection, Sep 4, 2015
Record Details
This FDA Inspection record concerns Qspex Technologies, Inc., with an inspection on September 4, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Qspex Technologies, Inc.
- Inspection Date
- September 4, 2015
- Product Type
- Devices
View Company Profile
ID · 59145915-7f87-4d05-869d-4433718209e0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 940880
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.250(b)Sampling plans
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