FDA Inspection 1220467 — Steri-Tek, LLC

Steri-Tek, LLC — FEI 3024987432

The FDA completed an inspection of Steri-Tek, LLC on September 26, 2023 in Lewisville, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 26, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Lewisville, TX (United States)