FDA Warning Letter — LifeCell Corporation

Case 40059 — FEI 1000306051

The FDA took a Warning Letter action against LifeCell Corporation on October 10, 2008 (Branchburg, NJ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
LifeCell Corporation
Date
October 10, 2008
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Branchburg, NJ (United States)