FDA Inspection 796226 — KBI Biopharma, Inc.

KBI Biopharma, Inc. — FEI 3004638264

The FDA completed an inspection of KBI Biopharma, Inc. on August 29, 2012 in Durham, NC. 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
August 29, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Durham, NC (United States)