FDA Warning Letter — A.R.C. LASER GMBH

Case 418642 — FEI 3006617841

The FDA took a Warning Letter action against A.R.C. LASER GMBH on May 21, 2014 (Nuremberg, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
A.R.C. LASER GMBH
Date
May 21, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Nuremberg (Germany)