FDA inspection

Getinge Disinfection Ab: FDA inspection ending Sep 19, 2013

FDA inspection 848822 · No Action Indicated (NAI) · Vaxjo

Key facts

Inspection ID 848822
Firm Getinge Disinfection Ab
FEI number 3000231474
Address Ljungadalsgatan 11
City Vaxjo
Country Sweden
Fiscal year 2013
Inspection end date Sep 19, 2013
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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