FDA Inspection
Jeffery M. Adelglass, M.D.Jeffery M. Adelglass, M.D. – FDA Inspection, Apr 24, 2012
Record Details
This FDA Inspection record concerns Jeffery M. Adelglass, M.D., with an inspection on April 24, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Jeffery M. Adelglass, M.D.
- Inspection Date
- April 24, 2012
- Product Type
- Devices
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ID · 5745de1f-32c4-4afc-a3b8-17ed40879254
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 778338
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(ii)Investigator adverse effect records inadequate
- 21 CFR 812.100No investigator protection - subject rights, safety, welfare
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Other FDA inspections of Jeffery M. Adelglass, M.D.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 17, 2025 | VAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
| October 4, 2019 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Jeffery M. Adelglass, M.D.
- FDA Inspection 1259031 - 2025-01-17
- FDA Inspection 1109131 - 2019-10-04
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