FDA inspection

Orion Corporation, Orion Pharma: FDA inspection ending Apr 21, 2017

FDA inspection 1012832 · Voluntary Action Indicated (VAI) · Espoo

Key facts

Inspection ID 1012832
Firm Orion Corporation, Orion Pharma
FEI number 3003073605
Address Orionintie 1
City Espoo
Country Finland
Fiscal year 2017
Inspection end date Apr 21, 2017
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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