FDA Inspection 958050 — Xytex Laboratories

Xytex Laboratories — FEI 1000507143

The FDA completed an inspection of Xytex Laboratories on February 2, 2016 in Augusta, GA. 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
February 2, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Augusta, GA (United States)