FDA Warning Letter — Leisegang Feinmechanick-Optik GmbH

Case 305239 — FEI 3002807462

The FDA took a Warning Letter action against Leisegang Feinmechanick-Optik GmbH on July 11, 2012 (Berlin, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Leisegang Feinmechanick-Optik GmbH
Date
July 11, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Berlin (Germany)