FDA Inspection 1327036 — Hospira Zagreb d.o.o.

Hospira Zagreb d.o.o. — FEI 3010630287

The FDA completed an inspection of Hospira Zagreb d.o.o. on July 23, 2024 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
July 23, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brdovec (Croatia)

Additional Details

Mutual Recognition Agreement (MRA)