FDA Inspection 1224385 — STERITECH, INC.

STERITECH, INC. — FEI 2648209

The FDA completed an inspection of STERITECH, INC. on December 8, 2023 in Salinas, PR. 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
December 8, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Salinas, PR (United States)

Citations

IDCFRDescription
322421 CFR 820.70(g)(2)Periodic equipment inspection lack of or inadequate procedu