FDA Inspection 1051780 — Hospira Zagreb d.o.o.
The FDA completed an inspection of Hospira Zagreb d.o.o. on February 20, 2018 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
- February 20, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Brdovec (Croatia)