FDA Inspection 711591 — Hospira, Inc.
The FDA completed an inspection of Hospira, Inc. on January 25, 2011 in Clayton, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 25, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Clayton, NC (United States)