FDA Inspection 1243197 — Xytex Laboratories

Xytex Laboratories — FEI 3019356415

The FDA completed an inspection of Xytex Laboratories on Jun 26, 2024 in Charlotte, NC. 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 26, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Charlotte, NC (United States)