FDA inspection

Delta Med SpA: FDA inspection ending May 3, 2012

FDA inspection 780033 · Voluntary Action Indicated (VAI) · Viadana

Key facts

Inspection ID 780033
Firm Delta Med SpA
FEI number 3006846316
Address Via Guido Rossa 20
City Viadana
Country Italy
Fiscal year 2012
Inspection end date May 3, 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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