# Vitalgo Inc. – FDA Inspection, Feb 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalgo-inc/b8e75582-fe15-494b-a107-f70edbb7c171
Source feed: FDA_Inspections

> FDA inspection 1028775 of Vitalgo Inc., February 17, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028775
- Company Name: Vitalgo Inc.
- Inspection Date: 2017-02-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1340152 - 2026-10-06
- [FDA Inspection 1259206 - 2024-12-13](https://www.keypedia.com/records/fda_inspections/vitalgo-inc/5c7d57c7-fd12-4b02-9aeb-e7d6fdfa1471)
- FDA Inspection 1182276 - 2022-10-27
- [FDA Inspection 928196 - 2015-05-28](https://www.keypedia.com/records/fda_inspections/vitalgo-inc/f57c42e2-ebc5-4299-8517-469d66556c96)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/vitalgo-inc/b9738159-1119-4c89-a095-1f81d2153ec2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7