FDA Inspection
Jon G. Dishler, M.D.Jon G. Dishler, M.D. – FDA Inspection, Apr 2, 2014
Record Details
This FDA Inspection record concerns Jon G. Dishler, M.D., with an inspection on April 2, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Jon G. Dishler, M.D.
- Inspection Date
- April 2, 2014
- Product Type
- Devices
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ID · b536cd39-b361-4933-b037-7974a354182f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 873239
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.7(a)Promotion or test marketing
- 21 CFR 812.100Investigator lack of informed consent
- 21 CFR 812.110(a)Subject participation prior to study approval
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Other FDA inspections of Jon G. Dishler, M.D.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 27, 2024 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 3, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 27, 2010 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Jon G. Dishler, M.D.
- FDA Inspection 1235869 - 2024-03-27
- FDA Inspection 965392 - 2016-03-03
- FDA Inspection 678710 - 2010-08-27
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