FDA Inspection 1088699 — Fuzion Medical

Fuzion Medical — FEI 3008284898

The FDA completed an inspection of Fuzion Medical on April 3, 2019 in Torrance, CA. 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
April 3, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Torrance, CA (United States)