FDA Inspection
Vesta Inc.Vesta Inc. – FDA Inspection, Jul 20, 2017
Record Details
This FDA Inspection record concerns Vesta Inc., with an inspection on July 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fd064182-9743-40ae-af0b-8c98d22972c7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1019861
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Vesta Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 13, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 31, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 20, 2017 | VAI | Center for Devices and Radiological Health | Project Evaluation: Devices |
| May 20, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Vesta Inc.
- FDA Inspection 1264302 - 2025-03-13
- FDA Inspection 1118871 - 2020-01-31
- FDA Inspection 1030227 - 2017-10-20
- FDA Inspection 880201 - 2014-05-20
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