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FDA Inspection 780147 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA completed an inspection of Roche Diagnostics GmbH on April 26, 2012 in Mannheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

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

Facility

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