FDA Inspection 940632 — STERIS CORPORATION
The FDA completed an inspection of STERIS CORPORATION on September 4, 2015 in Franklin Park, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 4, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Franklin Park, IL (United States)