FDA Inspection 1071119 — Vasundhara Cheekati

Vasundhara Cheekati — FEI 3014598762

The FDA completed an inspection of Vasundhara Cheekati on Sep 21, 2018 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)
End Date
Sep 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Clinical Investigator (CI)