FDA Inspection 1006128 — Wells Johnson Company

Wells Johnson Company — FEI 2024022

The FDA completed an inspection of Wells Johnson Company on March 22, 2017 in Tucson, AZ. 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
March 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Tucson, AZ (United States)

Citations

IDCFRDescription
243121 CFR 820.30(b)Design plans- updated