FDA inspection

Suanfarma Italia S.p.A.: FDA inspection ending May 9, 2019

FDA inspection 1129330 · Voluntary Action Indicated (VAI) · Rovereto

Key facts

Inspection ID 1129330
Firm Suanfarma Italia S.p.A.
FEI number 1000312133
Address Corso Verona 165
City Rovereto
Country Italy
Fiscal year 2019
Inspection end date May 9, 2019
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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