FDA Inspection 827576 — Kemper Drug

Kemper Drug — FEI 3008800413

The FDA completed an inspection of Kemper Drug on Mar 26, 2013 in Elk River, MN. 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
Mar 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Elk River, MN (United States)

Additional Details

Clinical Investigator (CI)