FDA Inspection 1123692 — Hospira Zagreb d.o.o.

Hospira Zagreb d.o.o. — FEI 3010630287

The FDA completed an inspection of Hospira Zagreb d.o.o. on March 22, 2019 in Brdovec. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brdovec (Croatia)

Additional Details

Mutual Recognition Agreement (MRA)