FDA Inspection 1091387 — Hoosier, Inc

Hoosier, Inc — FEI 3003058119

The FDA completed an inspection of Hoosier, Inc on May 31, 2019 in Corona, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 31, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Corona, CA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation