FDA inspection

Lavipharm S.A.: FDA inspection ending Oct 19, 2020

FDA inspection 1193897 · Voluntary Action Indicated (VAI) · Paiania

Key facts

Inspection ID 1193897
Firm Lavipharm S.A.
FEI number 3001134933
Address Attica, Agias Marinas Street, Pobox 59
City Paiania
Country Greece
Fiscal year 2021
Inspection end date Oct 19, 2020
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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