FDA Inspection 790026 — Damien Sanderlin, MD

Damien Sanderlin, MD — FEI 3009417634

The FDA completed an inspection of Damien Sanderlin, MD on July 18, 2012 in Houston, TX. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 18, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Houston, TX (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
296921 CFR 812.100No investigator protection - subject rights, safety, welfare