FDA Inspection
Scripps IRBScripps IRB – FDA Inspection, Nov 2, 2009
Record Details
This FDA Inspection record concerns Scripps IRB, with an inspection on November 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Scripps IRB
- Inspection Date
- November 2, 2009
- Product Type
- Devices
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ID · d7a7674c-b7c7-4b46-be41-3d8865de2775
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 628279
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
4- 21 CFR 56.115(a)(5)List of members
- 21 CFR 56.115(a)(2)Minutes of IRB meetings
- 21 CFR 56.108(a)(1)Initial and continuing reviews
- 21 CFR 56.107(d)One non-affiliate member
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Other FDA inspections of Scripps IRB
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2025 | Not classified | Los Angeles District Office | |
| August 13, 2021 | NAI | Bioresearch Monitoring | |
| March 27, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Scripps IRB
- FDA Inspection 1277749 - 2025-07-30
- FDA Inspection 1150444 - 2021-08-13
- FDA Inspection 920650 - 2015-03-27
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