FDA Inspection
Jon G. Dishler, M.D.Jon G. Dishler, M.D. – FDA Inspection, Aug 27, 2010
Record Details
This FDA Inspection record concerns Jon G. Dishler, M.D., with an inspection on August 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Jon G. Dishler, M.D.
- Inspection Date
- August 27, 2010
- Product Type
- Devices
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ID · 5cb22c02-ad23-46ad-a7ce-bc55ea448948
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 678710
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
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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 |
| April 2, 2014 | 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 873239 - 2014-04-02
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