FDA Warning Letter — Gambro Dialysatoren GmbH

Case 74544 — FEI 3002807035

The FDA took a Warning Letter action against Gambro Dialysatoren GmbH on Sep 4, 2009 (Hechingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
Gambro Dialysatoren GmbH
Date
Sep 4, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Hechingen (Germany)

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