FDA inspection

RAUMEDIC Estonia AS: FDA inspection ending Jan 29, 2013

FDA inspection 819197 · No Action Indicated (NAI) · Tallinn

Key facts

Inspection ID 819197
Firm RAUMEDIC Estonia AS
FEI number 3008264255
Address Kadaka tee 46a
City Tallinn
Country Estonia
Fiscal year 2013
Inspection end date Jan 29, 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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