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FDA Inspection 781526 — Catalent Greenville Inc

Catalent Greenville Inc — FEI 3000209735

The FDA completed an inspection of Catalent Greenville Inc on May 11, 2012 in Greenville, NC. 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
May 11, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, NC (United States)

Facility

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FDA data resources