FDA Inspection 1054436 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806560

The FDA completed an inspection of Roche Diagnostics GmbH on April 12, 2018 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
April 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Penzberg (Germany)