FDA Inspection 859902 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA completed an inspection of Roche Diagnostics GmbH on December 18, 2013 in Mannheim. 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
December 18, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Postmarket Audit Inspections