FDA Inspection 1266713 — Steris Corporation

Steris Corporation — FEI 3016271578

The FDA completed an inspection of Steris Corporation on Apr 1, 2025 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 1, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)

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