FDA Inspection 780147 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA completed an inspection of Roche Diagnostics GmbH on Apr 26, 2012 in Mannheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 26, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mannheim (Germany)

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