FDA inspection

Leica Microsystems: FDA inspection ending May 20, 2003

FDA inspection 272199 · No Action Indicated (NAI) · Richmond, IL

Key facts

Inspection ID 272199
Firm Leica Microsystems
FEI number 1000124146
Address 5205 US Highway 12
City Richmond
State IL
ZIP 60071-9730
Fiscal year 2003
Inspection end date May 20, 2003
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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