FDA Inspection
Veniti, Inc.Veniti, Inc. – FDA Inspection, Jul 20, 2018
Record Details
This FDA Inspection record concerns Veniti, Inc., with an inspection on July 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e1797d7a-ac1f-4c23-9593-e24cfc485938
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1059665
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.75(a)Lack of or inadequate process validation
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Other FDA inspections of Veniti, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 21, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Veniti, Inc.
- FDA Inspection 879437 - 2014-05-21
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