FDA Inspection 667066 — VisionGift

VisionGift — FEI 3001239138

The FDA completed an inspection of VisionGift on Jun 16, 2010 in Portland, OR. 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 16, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Portland, OR (United States)

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