FDA inspection

Leica Microsystems (Schweiz) Ag: FDA inspection ending Dec 8, 2011

FDA inspection 765055 · Voluntary Action Indicated (VAI) · Heerbrugg

Key facts

Inspection ID 765055
Firm Leica Microsystems (Schweiz) Ag
FEI number 3003974370
Address Max Schmidheiny-Strasse 201
City Heerbrugg
Country Switzerland
Fiscal year 2012
Inspection end date Dec 8, 2011
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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