FDA Inspection 836295 — Catalent Indiana, LLC

Catalent Indiana, LLC — FEI 3005949964

The FDA completed an inspection of Catalent Indiana, LLC on Jun 17, 2013 in Bloomington, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 17, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bloomington, IN (United States)