FDA Inspection 869531 — Life Line Stem Cell, Inc.

Life Line Stem Cell, Inc. — FEI 3009192463

The FDA completed an inspection of Life Line Stem Cell, Inc. on March 6, 2014 in New Haven, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 6, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
New Haven, IN (United States)