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FDA Inspection
•Eversight•March 25, 2011

Eversight – FDA Inspection, Mar 25, 2011

Record Details

This FDA Inspection record concerns Eversight, with an inspection on March 25, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Eversight
Inspection Date
March 25, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · e834372f-be77-438e-9fd9-f55773266da8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
716940
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

3
  1. 21 CFR 1271.47(d)Departures: recording and justifying
  2. 21 CFR 1271.195(d)Documentation not maintained
  3. 21 CFR 1271.160(b)(6)Deviations--evaluation, cause, corrective action

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Eversight

6
DateClassificationOfficeProject area
July 29, 2026NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 5, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 25, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 27, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 24, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Eversight
  • FDA Inspection 1330724 - 2026-07-29
  • FDA Inspection 1192811 - 2022-12-05
  • FDA Inspection 1084752 - 2019-03-25
  • FDA Inspection 978214 - 2016-07-27
  • FDA Inspection 888328 - 2014-07-24

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