# Hoosier, Inc – FDA Inspection, May 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/hoosier-inc/e7d57146-3a6e-4b69-bb7c-c82513c79783
Source feed: FDA_Inspections

> FDA inspection 1091387 of Hoosier, Inc, May 31, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 1091387
- Company Name: Hoosier, Inc
- Inspection Date: 2019-05-31
- 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 1279077 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/hoosier-inc/d5393340-edc6-4eda-9b98-158f7a3fa0af)

## Related Officers

- [Investigator](https://www.keypedia.com/people/kevin-n-tran/dd74120c-4a8d-4fd0-9068-c862890d00d6)

Company: https://www.keypedia.com/companies/hoosier-inc/0f6d66b1-20e6-402c-842f-a8a49ec4b80b

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