FDA inspection

bioMerieux Italia SpA: FDA inspection ending Jun 15, 2017

FDA inspection 1019450 · Voluntary Action Indicated (VAI) · Bagno A Ripoli

Key facts

Inspection ID 1019450
Firm bioMerieux Italia SpA
FEI number 3003261083
Address Via Di Gamorglaino, 58 Loc Ponte A Ema
City Bagno A Ripoli
Country Italy
Fiscal year 2017
Inspection end date Jun 15, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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