FDA Warning Letter — Tetracore, Inc.

Case 86204 — FEI 3003517954

The FDA took a Warning Letter action against Tetracore, Inc. on December 1, 2009 (Rockville, MD). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Tetracore, Inc.
Date
December 1, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Rockville, MD (United States)