FDA inspection

Sorin Group Italia S.r.l.: FDA inspection ending Nov 30, 2017

FDA inspection 1050264 · No Action Indicated (NAI) · Saluggia

Key facts

Inspection ID 1050264
Firm Sorin Group Italia S.r.l.
FEI number 3005687633
Address Via Crescentino Sn
City Saluggia
Fiscal year 2018
Inspection end date Nov 30, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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