FDA Inspection 750025 — Manish Mehta, MD

Manish Mehta, MD — FEI 3009579540

The FDA completed an inspection of Manish Mehta, MD on October 24, 2011 in Albany, NY. 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
October 24, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Albany, NY (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
292821 CFR 812.40Sponsors' general responsibilities
723121 CFR 50.20Consent not obtained, exceptions do not apply