FDA inspection

Przedsiebiorstwo Farmaceutyczne Jelfa SA: FDA inspection ending May 15, 2012

FDA inspection 794037 · Voluntary Action Indicated (VAI) · Jelenia Gora

Key facts

Inspection ID 794037
Firm Przedsiebiorstwo Farmaceutyczne Jelfa SA
FEI number 3004680543
Address Ul. Wincentego Pola 21
City Jelenia Gora
Country Poland
Fiscal year 2012
Inspection end date May 15, 2012
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 10–99 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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