FDA Inspection 792362 — Manish Mehta, MD

Manish Mehta, MD — FEI 3009579540

The FDA completed an inspection of Manish Mehta, MD on July 9, 2012 in Albany, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Albany, NY (United States)

Additional Details

Clinical Investigator (CI)