FDA Inspection
John H. Joseph, M.DJohn H. Joseph, M.D – FDA Inspection, Jun 28, 2017
Record Details
This FDA Inspection record concerns John H. Joseph, M.D, with an inspection on June 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a2965d9f-d4d0-48bd-b9e1-da1affd8ce02
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1016204
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of John H. Joseph, M.D
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 12, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 13, 2020 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 25, 2014 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 23, 2009 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
Other documents for John H. Joseph, M.D
- FDA Inspection 1202752 - 2023-04-12
- FDA Inspection 1122362 - 2020-03-13
- FDA Inspection 893898 - 2014-08-25
- FDA Inspection 615210 - 2009-09-23
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