FDA Inspection 1220467 — Steri-Tek, LLC

Steri-Tek, LLC — FEI 3024987432

The FDA completed an inspection of Steri-Tek, LLC on Sep 26, 2023 in Lewisville, TX. 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). Product area: Devices.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.