FDA Warning Letter — VBM Medizintechnik GmbH

Case 138933 — FEI 3002808440

The FDA took a Warning Letter action against VBM Medizintechnik GmbH on December 7, 2010 (Sulz Am Neckar, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
VBM Medizintechnik GmbH
Date
December 7, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Sulz Am Neckar (Germany)