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FDA Inspection 983864 — Veranova LP

Veranova LP — FEI 2018076

The FDA completed an inspection of Veranova LP on September 2, 2016 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
September 2, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Devens, MA (United States)

Facility

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  • 859015 (NAI Mon Dec 02 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 752347 (VAI Mon Nov 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 651722 (NAI Fri Feb 26 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources