FDA Inspection
VisionGiftVisionGift – FDA Inspection, Apr 29, 2016
Record Details
This FDA Inspection record concerns VisionGift, with an inspection on April 29, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- VisionGift
- Inspection Date
- April 29, 2016
- Product Type
- Biologics
View Company Profile
ID · 7d953743-4342-4d22-8793-203e001101f1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 968164
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.50(a)Determination based on screening and testing
Full citation text and observation details available on the Dashboard.
Other FDA inspections of VisionGift
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 4, 2023 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 25, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 18, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| December 2, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 16, 2010 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for VisionGift
- FDA Inspection 1225569 - 2023-12-04
- FDA Inspection 1102889 - 2019-09-25
- FDA Inspection 895861 - 2014-09-18
- FDA Inspection 756331 - 2011-12-02
- FDA Inspection 667066 - 2010-06-16
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