FDA Warning Letter — EPflex Feinwerktechnik GmbH

Case 409621 — FEI 3003289691

The FDA took a Warning Letter action against EPflex Feinwerktechnik GmbH on September 16, 2013 (Dettingen An Der Erms, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
EPflex Feinwerktechnik GmbH
Date
September 16, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Dettingen An Der Erms (Germany)