FDA Inspection 1281950 — STERIS Schweiz AG

STERIS Schweiz AG — FEI 3002808269

The FDA completed an inspection of STERIS Schweiz AG on January 24, 2024 in Daniken. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Daniken (Switzerland)

Additional Details

Mutual Recognition Agreement (MRA)