# Vitalconnect Inc. – FDA Inspection, Jul 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/vitalconnect-inc/d82dcbd3-26d4-439f-95b7-e86a4770f6c6
Source feed: FDA_Inspections

> FDA inspection 1097585 of Vitalconnect Inc., July 25, 2019. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097585
- Company Name: Vitalconnect Inc.
- Inspection Date: 2019-07-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1231015 - 2024-02-15

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)
- [Issuing Officer](https://www.keypedia.com/people/tuan-a-nguyen/50723bbb-29a1-4e7a-a5aa-123ec3866065)

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