FDA inspection

Hospira Zagreb d.o.o.: FDA inspection ending Feb 20, 2018

FDA inspection 1051780 · Voluntary Action Indicated (VAI) · Brdovec

Key facts

Inspection ID 1051780
Firm Hospira Zagreb d.o.o.
FEI number 3010630287
Address Prudnicka Cesta 60
City Brdovec
Country Croatia
Fiscal year 2018
Inspection end date Feb 20, 2018
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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