FDA Inspection 873239 — Jon G. Dishler, M.D.

Jon G. Dishler, M.D. — FEI 1000517653

The FDA completed an inspection of Jon G. Dishler, M.D. on Apr 2, 2014 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 2, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Greenwood Village, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
291021 CFR 812.7(a)Promotion or test marketing
297021 CFR 812.100Investigator lack of informed consent
297321 CFR 812.110(a)Subject participation prior to study approval