# FDA Inspection 965392 - Jon G. Dishler, M.D. - March 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/jon-g-dishler-md/11108a3e-3b1f-445f-a59f-df74e5126c3f
Source feed: FDA_Inspections

> FDA Inspection 965392 for Jon G. Dishler, M.D. on March 03, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 965392
- Company Name: Jon G. Dishler, M.D.
- Inspection Date: 2016-03-03
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1235869 - 2024-03-27](https://www.keypedia.com/records/fda_inspections/jon-g-dishler-md/74266ae6-dcaa-477d-b7e6-d344853f761d)
- [FDA Inspection 873239 - 2014-04-02](https://www.keypedia.com/records/fda_inspections/jon-g-dishler-md/b536cd39-b361-4933-b037-7974a354182f)
- [FDA Inspection 678710 - 2010-08-27](https://www.keypedia.com/records/fda_inspections/jon-g-dishler-md/5cb22c02-ad23-46ad-a7ce-bc55ea448948)

Company: https://www.keypedia.com/companies/jon-g-dishler-md/243fb74e-6c36-4b5b-8caa-886672f0bf86

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
