FDA Inspection 940349 — KP Pharmaceutical Technology

KP Pharmaceutical Technology — FEI 3001802820

The FDA completed an inspection of KP Pharmaceutical Technology on May 21, 2015 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
May 21, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bloomington, IN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.