FDA Inspection 1005490 — Jason M. Perrin, MD

Jason M. Perrin, MD — FEI 3013198412

The FDA completed an inspection of Jason M. Perrin, MD on Mar 10, 2017 in Mannheim. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
298121 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
701221 CFR 812.100Investigator lack of control of investigational devices

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.