FDA inspection

MEGIN OY: FDA inspection ending Oct 27, 2016

FDA inspection 995999 · No Action Indicated (NAI) · Espoo

Key facts

Inspection ID 995999
Firm MEGIN OY
FEI number 3006563303
Address Siltasaarenkatu 18-20A, SILTASAARENKATU 18-20 A
City Espoo
Country Finland
Fiscal year 2017
Inspection end date Oct 27, 2016
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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