FDA Inspection 1221122 — Stephens Instruments, Inc

Stephens Instruments, Inc — FEI 1045379

The FDA completed an inspection of Stephens Instruments, Inc on Oct 26, 2023 in Lexington, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 26, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, KY (United States)

Citations

IDCFRDescription
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures