FDA inspection

Hemofarm AD Vrsac: FDA inspection ending May 8, 2015

FDA inspection 926320 · Voluntary Action Indicated (VAI) · Vrsac

Key facts

Inspection ID 926320
Firm Hemofarm AD Vrsac
FEI number 3006082102
Address Beogradski put bb
City Vrsac
Country Serbia
Fiscal year 2015
Inspection end date May 8, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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