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FDA Inspection 1019260 — Catalent Greenville Inc

Catalent Greenville Inc — FEI 3000209735

The FDA completed an inspection of Catalent Greenville Inc on April 13, 2017 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
April 13, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, NC (United States)

Facility

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FDA data resources