FDA Warning Letter — Dornier Medtech America, Inc.

Case 87984 — FEI 1037955

The FDA took a Warning Letter action against Dornier Medtech America, Inc. on March 23, 2010 (Kennesaw, GA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Dornier Medtech America, Inc.
Date
March 23, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Kennesaw, GA (United States)