FDA Inspection
Hospira, Inc.Hospira, Inc. – FDA Inspection, Nov 15, 2013
Record Details
This FDA Inspection record concerns Hospira, Inc., with an inspection on November 15, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hospira, Inc.
- Inspection Date
- November 15, 2013
- Product Type
- Devices
View Company Profile
ID · e5c9bb40-43fb-4ad5-a8b3-642e0ff86d62
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 855618
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Hospira, Inc.
12| Date | Classification | Office | Project area |
|---|---|---|---|
| February 7, 2025 | Not classified | Atlanta District Office | |
| November 14, 2023 | OAI | Atlanta District Office | |
| November 21, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 2, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 26, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Hospira, Inc.
- FDA Inspection 1251941 - 2025-02-07
- FDA Inspection 1223090 - 2023-11-14
- FDA Inspection 1110899 - 2019-11-21
- FDA Inspection 1039547 - 2018-02-02
- FDA Inspection 984874 - 2016-05-26
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