FDA inspection

STERIS Schweiz AG: FDA inspection ending Mar 3, 2010

FDA inspection 658610 · No Action Indicated (NAI) · Daniken

Key facts

Inspection ID 658610
Firm STERIS Schweiz AG
FEI number 3002808269
Address Hogenweidstrasse 6
City Daniken
Country Switzerland
Fiscal year 2010
Inspection end date Mar 3, 2010
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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