FDA Warning Letter — Hospira, Inc.

Case 422589 — FEI 1021343

The FDA took a Warning Letter action against Hospira, Inc. on March 7, 2014 (Rocky Mount, NC). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Hospira, Inc.
Date
March 7, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Rocky Mount, NC (United States)