FDA Inspection 678710 — Jon G. Dishler, M.D.

Jon G. Dishler, M.D. — FEI 1000517653

The FDA completed an inspection of Jon G. Dishler, M.D. on Aug 27, 2010 in Greenwood Village, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Greenwood Village, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations