FDA Inspection 801598 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806560

The FDA completed an inspection of Roche Diagnostics GmbH on Sep 20, 2012 in Penzberg. 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
Sep 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Penzberg (Germany)

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