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FDA Inspection 868435 — Catalent Germany Schorndorf GmbH

Catalent Germany Schorndorf GmbH — FEI 3003831171

The FDA completed an inspection of Catalent Germany Schorndorf GmbH on February 7, 2014 in Schorndorf. 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
February 7, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schorndorf (Germany)

Facility

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