FDA inspection

Suanfarma Italia S.p.A.: FDA inspection ending Jul 1, 2011

FDA inspection 738821 · Voluntary Action Indicated (VAI) · Rovereto

Key facts

Inspection ID 738821
Firm Suanfarma Italia S.p.A.
FEI number 1000312133
Address Corso Verona 165
City Rovereto
Country Italy
Fiscal year 2011
Inspection end date Jul 1, 2011
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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