FDA Inspection 796202 — Amit Mehta, MD

Amit Mehta, MD — FEI 3009531128

The FDA completed an inspection of Amit Mehta, MD on August 9, 2012 in San Antonio, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Antonio, TX (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
300721 CFR 812.140(d)Record retention inadequate
731921 CFR 56.115(a)(3)Records of continuing review