FDA Inspection 663036 — Eisenberg, Gerald, MD

Eisenberg, Gerald, MD — FEI 3004787974

The FDA completed an inspection of Eisenberg, Gerald, MD on May 19, 2010 in Morton Grove, IL. 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
May 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Morton Grove, IL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations