FDA inspection

Dipharma Francis Srl: FDA inspection ending Dec 20, 2010

FDA inspection 705342 · No Action Indicated (NAI) · Mereto Di Tomba

Key facts

Inspection ID 705342
Firm Dipharma Francis Srl
FEI number 3002806810
Address Via Ventiquattro Maggio 40
City Mereto Di Tomba
Country Italy
Fiscal year 2011
Inspection end date Dec 20, 2010
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections