FDA Inspection 732459 — Fareva Mirabel

Fareva Mirabel — FEI 1000173162

The FDA completed an inspection of Fareva Mirabel on May 23, 2011 in Riom. 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
May 23, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Riom (France)

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