FDA Warning Letter — Natus Europe GmbH

Case 394336 — FEI 3003118721

The FDA took a Warning Letter action against Natus Europe GmbH on Apr 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
Apr 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Planegg (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.