FDA inspection

Steris Corporation: FDA inspection ending Mar 31, 2022

FDA inspection 1165995 · Voluntary Action Indicated (VAI) · Saint Louis, MO

Key facts

Inspection ID 1165995
Firm Steris Corporation
FEI number 1923569
Address 5 Sunnen Dr
City Saint Louis
State MO
ZIP 63143
Country United States
Fiscal year 2022
Inspection end date Mar 31, 2022
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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