FDA inspection

Orion Corporation, Orion Pharma: FDA inspection ending Nov 2, 2012

FDA inspection 807739 · Administrative/Directed Change (ADC) · Espoo

Key facts

Inspection ID 807739
Firm Orion Corporation, Orion Pharma
FEI number 3003073605
Address Koivu-Mankkaan Tie 6b
City Espoo
Fiscal year 2013
Inspection end date Nov 2, 2012
Classification Administrative/Directed Change (ADC)
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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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