FDA Inspection 846339 — DRG Instruments GmbH

DRG Instruments GmbH — FEI 3002800697

The FDA completed an inspection of DRG Instruments GmbH on Aug 22, 2013 in Marburg. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Marburg (Germany)

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