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FDA Inspection
•Saving Sight•January 28, 2016

Saving Sight – FDA Inspection, Jan 28, 2016

Record Details

This FDA Inspection record concerns Saving Sight, with an inspection on January 28, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Saving Sight
Inspection Date
January 28, 2016
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · dc2a608d-219f-4144-9619-955602d39a78

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
957153
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.215Potential problems with recovery

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Saving Sight

5
DateClassificationOfficeProject area
April 16, 2025NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 15, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 2, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 15, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 13, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Saving Sight
  • FDA Inspection 1268860 - 2025-04-16
  • FDA Inspection 1042335 - 2018-02-15
  • FDA Inspection 881426 - 2014-06-02
  • FDA Inspection 781938 - 2012-05-15
  • FDA Inspection 671631 - 2010-07-13

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