FDA Inspection 697892 — Xytex Laboratories

Xytex Laboratories — FEI 1000507143

The FDA completed an inspection of Xytex Laboratories on Nov 17, 2010 in Augusta, GA. 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
Nov 17, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Augusta, GA (United States)

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