FDA Inspection 763386 — BioEden Inc

BioEden Inc — FEI 3005877419

The FDA completed an inspection of BioEden Inc on Jan 18, 2012 in Austin, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 18, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Austin, TX (United States)