FDA Inspection
Hoosier, IncHoosier, Inc – FDA Inspection, May 31, 2019
Record Details
This FDA Inspection record concerns Hoosier, Inc, with an inspection on May 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e7d57146-3a6e-4b69-bb7c-c82513c79783
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1091387
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(b)Documentation
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Other FDA inspections of Hoosier, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 21, 2025 | VAI | Los Angeles District Office | Compliance: Medical Devices |
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