FDA inspection

Immunodiagnostic Systems Sa: FDA inspection ending Nov 15, 2012

FDA inspection 809346 · No Action Indicated (NAI) · Liege

Key facts

Inspection ID 809346
Firm Immunodiagnostic Systems Sa
FEI number 3007500635
Address Rue Ernest-solvay 101
City Liege
Country Belgium
Fiscal year 2013
Inspection end date Nov 15, 2012
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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