FDA Inspection 1027867 — IntegoGen, LLC

IntegoGen, LLC — FEI 3012349839

The FDA completed an inspection of IntegoGen, LLC on June 12, 2017 in Tallahassee, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 12, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tallahassee, FL (United States)