FDA Inspection 633785 — Michael A. Jacobs, M.D.

Michael A. Jacobs, M.D. — FEI 3008010098

The FDA completed an inspection of Michael A. Jacobs, M.D. on Dec 17, 2009 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 17, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
723121 CFR 50.20Consent not obtained, exceptions do not apply