FDA Inspection 1057452 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA completed an inspection of Roche Diagnostics GmbH on Apr 19, 2018 in Mannheim. 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
Apr 19, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Mannheim (Germany)

Additional Details

Postmarket Audit Inspections

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