FDA inspection

FOTONA D.O.O.: FDA inspection ending May 14, 2015

FDA inspection 926390 · Voluntary Action Indicated (VAI) · Ljubljana

Key facts

Inspection ID 926390
Firm FOTONA D.O.O.
FEI number 1000597018
Address Stegne 7
City Ljubljana
Country Slovenia
Fiscal year 2015
Inspection end date May 14, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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