FDA inspection

3Shape Poland: FDA inspection ending Sep 26, 2013

FDA inspection 851801 · Voluntary Action Indicated (VAI) · Szczecin

Key facts

Inspection ID 851801
Firm 3Shape Poland
FEI number 3015172511
Address Ul. Poludniowa 27c
City Szczecin
Country Poland
Fiscal year 2013
Inspection end date Sep 26, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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