FDA inspection

Latina Pharma S.p.A.: FDA inspection ending Apr 21, 2017

FDA inspection 1018753 · Voluntary Action Indicated (VAI) · Sermoneta

Key facts

Inspection ID 1018753
Firm Latina Pharma S.p.A.
FEI number 3001229385
Address Via del Murillo Km 2,800
City Sermoneta
Country Italy
Fiscal year 2017
Inspection end date Apr 21, 2017
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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