FDA Warning Letter — Instrumed GmbH

Case 415984 — FEI 3007290840

The FDA took a Warning Letter action against Instrumed GmbH on Mar 28, 2014 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
Instrumed GmbH
Date
Mar 28, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)

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