FDA Inspection 1153027 — Sandeep K. Goyal , MD

Sandeep K. Goyal , MD — FEI 3017367029

The FDA completed an inspection of Sandeep K. Goyal , MD on September 17, 2021 in Atlanta, GA. 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
September 17, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Clinical Investigator (CI)