FDA inspection

DIMA ITALIA SRL: FDA inspection ending Jul 26, 2012

FDA inspection 794734 · Voluntary Action Indicated (VAI) · Bologna

Key facts

Inspection ID 794734
Firm DIMA ITALIA SRL
FEI number 3007123976
Address Via Coriolano Vighi 29
City Bologna
Country Italy
Fiscal year 2012
Inspection end date Jul 26, 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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