# InfoBionic, Inc. – FDA Inspection, Apr 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/infobionic-inc/6a7ac35e-65eb-4746-8edb-fad7dd913be3
Source feed: FDA_Inspections

> FDA inspection 1085891 of InfoBionic, Inc., April 10, 2019. Classification: Voluntary Action Indicated (VAI). 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: 1085891
- Company Name: InfoBionic, Inc.
- Inspection Date: 2019-04-10
- 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: 3

## Related Documents

- FDA Inspection 1194164 - 2022-11-17

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

Company: https://www.keypedia.com/companies/infobionic-inc/eacb0491-ba47-41dd-bfef-0b0062c9d473

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