# FDA Inspection 1028775 - Vitalgo Inc. - February 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalgo-inc/1f5cccdc-591b-4a6c-9ff0-cdedf515a530
Source feed: FDA_Inspections

> FDA Inspection 1028775 for Vitalgo Inc. on February 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028775
- Company Name: Vitalgo Inc.
- Inspection Date: 2017-02-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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