FDA Warning Letter — 3CPM Company., INC.- EndoSure, Inc.

Case 89144 — FEI 3002900388

The FDA took a Warning Letter action against 3CPM Company., INC.- EndoSure, Inc. on March 25, 2010 (Sparks Glenco, MD). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
3CPM Company., INC.- EndoSure, Inc.
Date
March 25, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Sparks Glenco, MD (United States)