FDA Inspection 1038659 — Raj P. Wadwa, MD

Raj P. Wadwa, MD — FEI 3008107081

The FDA completed an inspection of Raj P. Wadwa, MD on Jan 11, 2018 in Aurora, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 11, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aurora, CO (United States)

Additional Details

Clinical Investigator (CI)