FDA Warning Letter — Trokamed GmbH

Case 414184 — FEI 3004595684

The FDA took a Warning Letter action against Trokamed GmbH on November 22, 2013 (Geisingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Trokamed GmbH
Date
November 22, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Geisingen (Germany)