FDA Inspection
EversightEversight – FDA Inspection, Apr 2, 2014
Record Details
This FDA Inspection record concerns Eversight, with an inspection on April 2, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Eversight
- Inspection Date
- April 2, 2014
- Product Type
- Biologics
View Company Profile
ID · 606871a9-62d2-44df-974a-460cf8896b1e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 872698
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.250(c)All labeling requirements met
- 21 CFR 1271.230(a)Validation & approval--established procedures
- 21 CFR 1271.160(b)(1)Ensuring appropriate core requirements followed
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Other FDA inspections of Eversight
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 18, 2022 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| February 19, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 22, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 9, 2012 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| December 4, 2009 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Eversight
- FDA Inspection 1178408 - 2022-08-18
- FDA Inspection 1079760 - 2019-02-19
- FDA Inspection 986660 - 2016-09-22
- FDA Inspection 793821 - 2012-08-09
- FDA Inspection 632949 - 2009-12-04
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