FDA Warning Letter — Hospira Inc

Case 72523 — FEI 2921482

The FDA took a Warning Letter action against Hospira Inc on Aug 12, 2009 (Morgan Hill, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Hospira Inc
Date
Aug 12, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Morgan Hill, CA (United States)