# FDA Inspection 1231015 - Vitalconnect Inc. - February 15, 2024

Source: https://www.keypedia.com/records/fda_inspections/vitalconnect-inc/5f49005d-d449-4513-b37d-dbfd1d525bf9
Source feed: FDA_Inspections

> FDA Inspection 1231015 for Vitalconnect Inc. on February 15, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1231015
- Company Name: Vitalconnect Inc.
- Inspection Date: 2024-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1097585 - 2019-07-25](https://www.keypedia.com/records/fda_inspections/vitalconnect-inc/d140e1b7-9fea-445b-9869-14c766ba6f9a)
- [FDA Inspection 1097585 - 2019-07-25](https://www.keypedia.com/records/fda_inspections/vitalconnect-inc/d82dcbd3-26d4-439f-95b7-e86a4770f6c6)

Company: https://www.keypedia.com/companies/vitalconnect-inc/5b545623-a3d0-4848-aa65-887703f2c807

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