FDA Inspection 1148855 — VisionGift

VisionGift — FEI 3013534653

The FDA completed an inspection of VisionGift on Aug 13, 2021 in Boston, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 13, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Boston, MA (United States)

Citations

IDCFRDescription
1235721 CFR 1271.195(a)(1)Temperature and humidity controls

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