FDA Warning Letter — Hospira, Inc.

Case 506761 — FEI 1925262

The FDA took a Warning Letter action against Hospira, Inc. on February 14, 2017 (Mcpherson, KS). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Hospira, Inc.
Date
February 14, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Mcpherson, KS (United States)