FDA inspection

Eurospital S.P.A.: FDA inspection ending Feb 23, 2012

FDA inspection 770910 · Voluntary Action Indicated (VAI) · Trieste

Key facts

Inspection ID 770910
Firm Eurospital S.P.A.
FEI number 1000553563
Address Via Flavia 122
City Trieste
Country Italy
Fiscal year 2012
Inspection end date Feb 23, 2012
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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