FDA Warning Letter — NARVA Lichtquelle GmbH + Co. KG

Case 508514 — FEI 3002553648

The FDA took a Warning Letter action against NARVA Lichtquelle GmbH + Co. KG on February 23, 2017 (Berlin, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
NARVA Lichtquelle GmbH + Co. KG
Date
February 23, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Berlin (Germany)