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FDA Inspection 983236 — Catalent Greenville Inc

Catalent Greenville Inc — FEI 3000209735

The FDA completed an inspection of Catalent Greenville Inc on July 14, 2016 in Greenville, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, NC (United States)

Facility

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FDA data resources