FDA Inspection 801598 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806560

The FDA completed an inspection of Roche Diagnostics GmbH on September 20, 2012 in Penzberg. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Penzberg (Germany)

Additional Details

Postmarket Audit Inspections