FDA Inspection 1196557 — KP Pharmaceutical Technology

KP Pharmaceutical Technology — FEI 3001802820

The FDA completed an inspection of KP Pharmaceutical Technology on February 3, 2023 in Bloomington, IN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 3, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bloomington, IN (United States)