FDA inspection

Origio A/S: FDA inspection ending Mar 26, 2015

FDA inspection 921059 · Voluntary Action Indicated (VAI) · Malov

Key facts

Inspection ID 921059
Firm Origio A/S
FEI number 3004048494
Address Knardrupvej 2
City Malov
Country Denmark
Fiscal year 2015
Inspection end date Mar 26, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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