FDA Inspection 1058354 — LifeGift

LifeGift — FEI 3001238027

The FDA completed an inspection of LifeGift on Jun 7, 2018 in Lubbock, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 7, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lubbock, TX (United States)