FDA Inspection
Varex Imaging CorporationVarex Imaging Corporation – FDA Inspection, Nov 9, 2011
Record Details
This FDA Inspection record concerns Varex Imaging Corporation, with an inspection on November 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Varex Imaging Corporation
- Inspection Date
- November 9, 2011
- Product Type
- Devices
View Company Profile
ID · 9cfd0ac5-26dc-4127-837e-191a3b28ad07
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 755193
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.198(e)Records of complaint investigation
- 21 CFR 820.20(b)Lack of or inadequate organizational structure
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Varex Imaging Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 19, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 8, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 31, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Varex Imaging Corporation
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.