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FDA Inspection 752347 — Veranova LP

Veranova LP — FEI 2018076

The FDA completed an inspection of Veranova LP on November 7, 2011 in Devens, MA. 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
November 7, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Devens, MA (United States)

Facility

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FDA data resources