FDA Warning Letter — ACell, Inc

Case 392488 — FEI 3005920706

The FDA took a Warning Letter action against ACell, Inc on April 26, 2013 (Columbia, MD). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
ACell, Inc
Date
April 26, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Columbia, MD (United States)