# FDA Inspection 1091387 - Hoosier, Inc - 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 for Hoosier, Inc on May 31, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1091387
- Company Name: Hoosier, Inc
- Inspection Date: 2019-05-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1279077 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/hoosier-inc/d5393340-edc6-4eda-9b98-158f7a3fa0af)
- [FDA Inspection 1279077 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/hoosier-inc/ca17ef39-175a-4341-aefb-c21367f7f650)

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