FDA Inspection 953498 — Richard E. Ringel, M.D.

Richard E. Ringel, M.D. — FEI 3007335984

The FDA completed an inspection of Richard E. Ringel, M.D. on Dec 17, 2015 in Baltimore, MD. 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
Dec 17, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations