FDA Inspection
VirtexVirtex – FDA Inspection, Apr 19, 2024
Record Details
This FDA Inspection record concerns Virtex, with an inspection on April 19, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 705f70ed-b80a-468e-9d8d-86cadd791783
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1236405
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.
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Other FDA inspections of Virtex
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 12, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Virtex
- FDA Inspection 1102921 - 2019-09-12
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