FDA Inspection
EversightEversight – FDA Inspection, Feb 25, 2010
Record Details
This FDA Inspection record concerns Eversight, with an inspection on February 25, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Eversight
- Inspection Date
- February 25, 2010
- Product Type
- Biologics
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ID · cb409c0a-4840-4b56-a84b-f5aa2f421c70
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 649083
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
4- 21 CFR 1271.160(a)All core requirements covered in program
- 21 CFR 1271.195(d)Documentation not maintained
- 21 CFR 1271.47(a)Design of procedures to ensure compliance
- 21 CFR 1271.160(b)(6)Deviations--Investigation, documenting, trending
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Eversight
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 29, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| December 5, 2022 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 25, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 27, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 24, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
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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