FDA Inspection
Vitalgo Inc.Vitalgo Inc. – FDA Inspection, Feb 17, 2017
Record Details
This FDA Inspection record concerns Vitalgo Inc., with an inspection on February 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Paul A. Licata (Issuing Officer)
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ID · b8e75582-fe15-494b-a107-f70edbb7c171
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1028775
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(c)Investigation of device failures
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Other FDA inspections of Vitalgo Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 6, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 13, 2024 | Not classified | Florida District Office | |
| October 27, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 28, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Vitalgo Inc.
- FDA Inspection 1340152 - 2026-10-06
- FDA Inspection 1259206 - 2024-12-13
- FDA Inspection 1182276 - 2022-10-27
- FDA Inspection 928196 - 2015-05-28
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