FDA inspection

Dipharma Francis S.r.l.: FDA inspection ending Feb 23, 2018

FDA inspection 1095006 · Voluntary Action Indicated (VAI) · Caronno Pertusella

Key facts

Inspection ID 1095006
Firm Dipharma Francis S.r.l.
FEI number 3003270894
Address Via Origgio 23
City Caronno Pertusella
Country Italy
Fiscal year 2018
Inspection end date Feb 23, 2018
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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