FDA Inspection 1341332 — STERIS CORPORATION
The FDA completed an inspection of STERIS CORPORATION on Sep 24, 2026 in Franklin Park, IL. 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
- Sep 24, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Franklin Park, IL (United States)