FDA Warning Letter — Natus Europe GmbH

Case 394336 — FEI 3003118721

The FDA took a Warning Letter action against Natus Europe GmbH on April 19, 2013 (Planegg, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Natus Europe GmbH
Date
April 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Planegg (Germany)