FDA Inspection 1081723 — Vivek Reddy, M.D.

Vivek Reddy, M.D. — FEI 3015186868

The FDA completed an inspection of Vivek Reddy, M.D. on Mar 7, 2019 in New York, NY. 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
Mar 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New York, NY (United States)

Additional Details

Sponsor-Investigator (S-I)

Citations

IDCFRDescription
1452321 CFR 812.43(c)No investigator agreement
700621 CFR 812.43(c)(5)No financial disclosure info in investigator agreement

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