FDA Inspection 965392 — Jon G. Dishler, M.D.

Jon G. Dishler, M.D. — FEI 1000517653

The FDA completed an inspection of Jon G. Dishler, M.D. on Mar 3, 2016 in Greenwood Village, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 3, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Greenwood Village, CO (United States)

Additional Details

Clinical Investigator (CI)