FDA Inspection
Vesta Inc.Vesta Inc. – FDA Inspection, Oct 20, 2017
Record Details
This FDA Inspection record concerns Vesta Inc., with an inspection on October 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ddc20b10-f0f1-4d97-859d-18a911075def
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030227
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
- 21 CFR 820.75(a)Lack of or inadequate process validation
Full citation text and observation details available on the Dashboard.
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 |
| July 20, 2017 | NAI | Center for Devices and Radiological Health | Compliance: 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 1019861 - 2017-07-20
- FDA Inspection 880201 - 2014-05-20
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