FDA Inspection 568143 — Hatten Paul MD

Hatten Paul MD — FEI 3007304067

The FDA completed an inspection of Hatten Paul MD on Feb 24, 2009 in Vero Beach, FL. 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
Feb 24, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Vero Beach, FL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
722721 CFR 50.27(a)Consent form not approved/signed/dated