FDA Inspection 1123162 — STERIS Schweiz AG

STERIS Schweiz AG — FEI 3002808269

The FDA completed an inspection of STERIS Schweiz AG on March 5, 2020 in Daniken. 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
March 5, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Daniken (Switzerland)