FDA Inspection 1020161 — Chawla, Dr Atul

Chawla, Dr Atul — FEI 3009229301

The FDA completed an inspection of Chawla, Dr Atul on June 23, 2017 in West Des Moines, IA. 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
June 23, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
West Des Moines, IA (United States)

Additional Details

Clinical Investigator (CI)