FDA Inspection 919379 — Hospira, Inc.
The FDA completed an inspection of Hospira, Inc. on April 13, 2015 in Lake Forest, IL. 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
- April 13, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Lake Forest, IL (United States)
Additional Details
Sponsor, Contract Research Organization